Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.

Nisha Limaye; N. Revencu; N. Van Regemorter; M. Garzon; M. Bonduelle; W. Chung; M. D. Daras; M. C. Fahey; C. Garrett; Y. Gillerot; G. Gillessen-Kaesbach; A. Giménez-Arnau; F. Guzzetta; D. Battaglia; K. Heimda; W. Lissens; E. Taub; L. Van Maldergem; W. Van Paesschen; D. Wieczorek; N. W. Wood; L. Boon; M. Vikkula

Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.

Nisha Limaye^*, N. Revencu, N. Van Regemorter, M. Garzon, M. Bonduelle, W. Chung, M. D. Daras, M. C. Fahey, C. Garrett, Y. Gillerot, G. Gillessen-Kaesbach, A. Giménez-Arnau, F. Guzzetta, D. Battaglia, K. Heimda, W. Lissens, E. Taub, L. Van Maldergem, W. Van Paesschen, D. WieczorekN. W. Wood, L. Boon, M. Vikkula

^*Corresponding author for this work

Institute of Human Genetics

Original language	English
Journal	Human Genetics
Volume	122
Issue number	5
Pages (from-to)	549
Number of pages	1
ISSN	0340-6717
Publication status	Published - 12.2007

Research Areas and Centers

Research Area: Medical Genetics

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This output contributes to the following UN Sustainable Development Goals (SDGs)

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Limaye, N., Revencu, N., Van Regemorter, N., Garzon, M., Bonduelle, M., Chung, W., Daras, M. D., Fahey, M. C., Garrett, C., Gillerot, Y., Gillessen-Kaesbach, G., Giménez-Arnau, A., Guzzetta, F., Battaglia, D., Heimda, K., Lissens, W., Taub, E., Van Maldergem, L., Van Paesschen, W., ... Vikkula, M. (2007). Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation. Human Genetics, 122(5), 549.

@article{90a03b7b6dd5476c952345170443bb2a,

title = "Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.",

author = "Nisha Limaye and N. Revencu and {Van Regemorter}, N. and M. Garzon and M. Bonduelle and W. Chung and Daras, {M. D.} and Fahey, {M. C.} and C. Garrett and Y. Gillerot and G. Gillessen-Kaesbach and A. Gim{\'e}nez-Arnau and F. Guzzetta and D. Battaglia and K. Heimda and W. Lissens and E. Taub and {Van Maldergem}, L. and {Van Paesschen}, W. and D. Wieczorek and Wood, {N. W.} and L. Boon and M. Vikkula",

year = "2007",

month = dec,

language = "English",

volume = "122",

pages = "549",

journal = "Human Molecular Genetics",

issn = "0964-6906",

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Limaye, N, Revencu, N, Van Regemorter, N, Garzon, M, Bonduelle, M, Chung, W, Daras, MD, Fahey, MC, Garrett, C, Gillerot, Y, Gillessen-Kaesbach, G, Giménez-Arnau, A, Guzzetta, F, Battaglia, D, Heimda, K, Lissens, W, Taub, E, Van Maldergem, L, Van Paesschen, W, Wieczorek, D, Wood, NW, Boon, L & Vikkula, M 2007, 'Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.', Human Genetics, vol. 122, no. 5, pp. 549.

TY - JOUR

T1 - Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.

AU - Limaye, Nisha

AU - Revencu, N.

AU - Van Regemorter, N.

AU - Garzon, M.

AU - Bonduelle, M.

AU - Chung, W.

AU - Daras, M. D.

AU - Fahey, M. C.

AU - Garrett, C.

AU - Gillerot, Y.

AU - Gillessen-Kaesbach, G.

AU - Giménez-Arnau, A.

AU - Guzzetta, F.

AU - Battaglia, D.

AU - Heimda, K.

AU - Lissens, W.

AU - Taub, E.

AU - Van Maldergem, L.

AU - Van Paesschen, W.

AU - Wieczorek, D.

AU - Wood, N. W.

AU - Boon, L.

AU - Vikkula, M.

PY - 2007/12

Y1 - 2007/12

UR - http://www.scopus.com/inward/record.url?scp=42049119216&partnerID=8YFLogxK

M3 - Journal articles

C2 - 18380023

AN - SCOPUS:42049119216

VL - 122

SP - 549

JO - Human Molecular Genetics

JF - Human Molecular Genetics

SN - 0964-6906

IS - 5

ER -

Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation.

Research Areas and Centers

UN SDGs

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