TY - JOUR
T1 - Erratum: A missense variant in mitochondrial amidoxime reducing component 1 gene and protection against liver disease (PLoS Genet (2020) 16:4 (e1008629) DOI: 10.1371/journal.pgen.1008629)
AU - Emdin, Connor A.
AU - Haas, Mary E.
AU - Khera, Amit V.
AU - Aragam, Krishna
AU - Chaffin, Mark
AU - Klarin, Derek
AU - Hindy, George
AU - Jiang, Lan
AU - Wei, Wei Qi
AU - Feng, Qiping
AU - Karjalainen, Juha
AU - Havulinna, Aki
AU - Kiiskinen, Tuomo
AU - Bick, Alexander
AU - Ardissino, Diego
AU - Wilson, James G.
AU - Schunkert, Heribert
AU - McPherson, Ruth
AU - Watkins, Hugh
AU - Elosua, Roberto
AU - Bown, Matthew J.
AU - Samani, Nilesh J.
AU - Baber, Usman
AU - Erdmann, Jeanette
AU - Gupta, Namrata
AU - Danesh, John
AU - Saleheen, Danish
AU - Chang, Kyong Mi
AU - Vujkovic, Marijana
AU - Voight, Ben
AU - Damrauer, Scott
AU - Lynch, Julie
AU - Kaplan, David
AU - Serper, Marina
AU - Tsao, Philip
AU - Program, Million Veteran
AU - Mercader, Josep
AU - Hanis, Craig
AU - Daly, Mark
AU - Denny, Joshua
AU - Gabriel, Stacey
AU - Kathiresan, Sekar
N1 - Publisher Copyright:
© 2021 Emdin et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
PY - 2021/4/6
Y1 - 2021/4/6
N2 - In this article, the genetic variant PNPLA3 p.I148M is misreported in several sentences as PNPLA3 p.I48M. The variant TM6SF2 p.E167K is misreported in one sentence as TM6SF2 p. E40K. In the Introduction, the third sentence of the second paragraph: For example, PNPLA3 p.I48M and TM6SF2 p.E40K, although initially identified as associated with hepatic steatosis [9,10], strongly predispose to the development of alcoholic cirrhosis [11], non-alcoholic cirrhosis [12,13] and hepatitis C-related cirrhosis [14,15]. should read: For example, PNPLA3 p.I1148M and TM6SF2 p.E167K, although initially identified as associated with hepatic steatosis [9,10], strongly predispose to the development of alcoholic cirrhosis [11], non-alcoholic cirrhosis [12,13] and hepatitis C-related cirrhosis [14,15]. In the Results, the fourth sentence of the first paragraph: We examined the association of all-cause cirrhosis with six genetic variants previously reported to be associated with alcoholic or non-alcoholic cirrhosis: PNPLA3 I48M, TM6SF2 E167K, MBOAT7 rs641738, HSD17B13 rs72613567, HFE C282Y and SERPINA1 E366K [11,16,18,19]. should read: We examined the association of all-cause cirrhosis with six genetic variants previously reported to be associated with alcoholic or non-alcoholic cirrhosis: PNPLA3 I148M, TM6SF2 E167K, MBOAT7 rs641738, HSD17B13 rs72613567, HFE C282Y and SERPINA1 E366K [11,16,18,19]. In the Methods, the first sentence of the first paragraph: To examine whether known alcoholic and non-alcoholic cirrhosis variants associate with all-cause cirrhosis, we tested the association of six known cirrhosis variants (PNPLA3 I48M, TM6SF2 E167K, MBOAT7 rs641738, HSD17B13 rs72613567, HFE C282Y and SERPINA1 E366K [11,16,18,19]) with all-cause cirrhosis in UK Biobank (hospitalization or death due to ICD codes K70.2, K70.3, K70.4, K74.0, K74.1, K74.2, K74.6, K76.6, or I85). should read: To examine whether known alcoholic and non-alcoholic cirrhosis variants associate with all-cause cirrhosis, we tested the association of six known cirrhosis variants (PNPLA3 I148M, TM6SF2 E167K, MBOAT7 rs641738, HSD17B13 rs72613567, HFE C282Y and SERPINA1 E366K [11,16,18,19]) with all-cause cirrhosis in UK Biobank (hospitalization or death due to ICD codes K70.2, K70.3, K70.4, K74.0, K74.1, K74.2, K74.6, K76.6, or I85). There is an error in Table 1. The name p.I48M appears instead of p.I148M. There is an error in the label of S1 Fig. The name p.I48M appears instead of p.I148M. The authors have provided a corrected version here.
AB - In this article, the genetic variant PNPLA3 p.I148M is misreported in several sentences as PNPLA3 p.I48M. The variant TM6SF2 p.E167K is misreported in one sentence as TM6SF2 p. E40K. In the Introduction, the third sentence of the second paragraph: For example, PNPLA3 p.I48M and TM6SF2 p.E40K, although initially identified as associated with hepatic steatosis [9,10], strongly predispose to the development of alcoholic cirrhosis [11], non-alcoholic cirrhosis [12,13] and hepatitis C-related cirrhosis [14,15]. should read: For example, PNPLA3 p.I1148M and TM6SF2 p.E167K, although initially identified as associated with hepatic steatosis [9,10], strongly predispose to the development of alcoholic cirrhosis [11], non-alcoholic cirrhosis [12,13] and hepatitis C-related cirrhosis [14,15]. In the Results, the fourth sentence of the first paragraph: We examined the association of all-cause cirrhosis with six genetic variants previously reported to be associated with alcoholic or non-alcoholic cirrhosis: PNPLA3 I48M, TM6SF2 E167K, MBOAT7 rs641738, HSD17B13 rs72613567, HFE C282Y and SERPINA1 E366K [11,16,18,19]. should read: We examined the association of all-cause cirrhosis with six genetic variants previously reported to be associated with alcoholic or non-alcoholic cirrhosis: PNPLA3 I148M, TM6SF2 E167K, MBOAT7 rs641738, HSD17B13 rs72613567, HFE C282Y and SERPINA1 E366K [11,16,18,19]. In the Methods, the first sentence of the first paragraph: To examine whether known alcoholic and non-alcoholic cirrhosis variants associate with all-cause cirrhosis, we tested the association of six known cirrhosis variants (PNPLA3 I48M, TM6SF2 E167K, MBOAT7 rs641738, HSD17B13 rs72613567, HFE C282Y and SERPINA1 E366K [11,16,18,19]) with all-cause cirrhosis in UK Biobank (hospitalization or death due to ICD codes K70.2, K70.3, K70.4, K74.0, K74.1, K74.2, K74.6, K76.6, or I85). should read: To examine whether known alcoholic and non-alcoholic cirrhosis variants associate with all-cause cirrhosis, we tested the association of six known cirrhosis variants (PNPLA3 I148M, TM6SF2 E167K, MBOAT7 rs641738, HSD17B13 rs72613567, HFE C282Y and SERPINA1 E366K [11,16,18,19]) with all-cause cirrhosis in UK Biobank (hospitalization or death due to ICD codes K70.2, K70.3, K70.4, K74.0, K74.1, K74.2, K74.6, K76.6, or I85). There is an error in Table 1. The name p.I48M appears instead of p.I148M. There is an error in the label of S1 Fig. The name p.I48M appears instead of p.I148M. The authors have provided a corrected version here.
UR - http://www.scopus.com/inward/record.url?scp=85103994754&partnerID=8YFLogxK
UR - https://www.mendeley.com/catalogue/faf7f970-99d5-3302-a295-56b748f24ef9/
U2 - 10.1371/journal.pgen.1009503
DO - 10.1371/journal.pgen.1009503
M3 - Comments/Debates
C2 - 33822779
AN - SCOPUS:85103994754
SN - 1553-7390
VL - 17
SP - e1009503
JO - PLoS Genetics
JF - PLoS Genetics
IS - 4
M1 - 1009503
ER -