TY - JOUR
T1 - Encephalopathy caused by novel mutations in the CMP-sialic acid transporter, SLC35A1
AU - University of Washington Center for Mendelian Genomics
AU - Ng, Bobby G.
AU - Asteggiano, Carla G.
AU - Kircher, Martin
AU - Buckingham, Kati J.
AU - Raymond, Kimiyo
AU - Nickerson, Deborah A.
AU - Shendure, Jay
AU - Bamshad, Michael J.
AU - Ensslen, Matthias
AU - Freeze, Hudson H.
N1 - Publisher Copyright:
© 2017 Wiley Periodicals, Inc.
PY - 2017/11
Y1 - 2017/11
N2 - Transport of activated nucleotide-sugars into the Golgi is critical for proper glycosylation and mutations in these transporters cause a group of rare genetic disorders termed congenital disorders of glycosylation. We performed exome sequencing on an individual with a profound neurological presentation and identified rare compound heterozygous mutations, p.Thr156Arg and p.Glu196Lys, in the CMP-sialic acid transporter, SLC35A1. Patient primary fibroblasts and serum showed a considerable decrease in the amount of N- and O-glycans terminating in sialic acid. Direct measurement of CMP-sialic acid transport into the Golgi showed a substantial decrease in overall rate of transport. Here we report the identification of the third patient with CMP-sialic acid transporter deficiency, who presented with severe neurological phenotype, but without hematological abnormalities.
AB - Transport of activated nucleotide-sugars into the Golgi is critical for proper glycosylation and mutations in these transporters cause a group of rare genetic disorders termed congenital disorders of glycosylation. We performed exome sequencing on an individual with a profound neurological presentation and identified rare compound heterozygous mutations, p.Thr156Arg and p.Glu196Lys, in the CMP-sialic acid transporter, SLC35A1. Patient primary fibroblasts and serum showed a considerable decrease in the amount of N- and O-glycans terminating in sialic acid. Direct measurement of CMP-sialic acid transport into the Golgi showed a substantial decrease in overall rate of transport. Here we report the identification of the third patient with CMP-sialic acid transporter deficiency, who presented with severe neurological phenotype, but without hematological abnormalities.
UR - http://www.scopus.com/inward/record.url?scp=85028577285&partnerID=8YFLogxK
U2 - 10.1002/ajmg.a.38412
DO - 10.1002/ajmg.a.38412
M3 - Journal articles
C2 - 28856833
AN - SCOPUS:85028577285
SN - 1552-4825
VL - 173
SP - 2906
EP - 2911
JO - American Journal of Medical Genetics, Part A
JF - American Journal of Medical Genetics, Part A
IS - 11
ER -