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 & 3 others N. W. Wood, L. Boon, M. Vikkula

Research output: Contribution to journalArticleResearchpeer-review

Original languageEnglish
Number of pages1
JournalHuman Genetics
Volume122
Issue number5
Publication statusPublished - 1 Dec 2007

Cite this

Limaye, N., Revencu, N., Van Regemorter, N., Garzon, M., Bonduelle, M., Chung, W., ... Vikkula, M. (2007). Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation. Human Genetics, 122(5).
Limaye, Nisha ; 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. ; Wieczorek, D. ; Wood, N. W. ; Boon, L. ; Vikkula, M. / Novel human pathological mutations. Gene symbol : KRIT1. Disease: cerebral cavernous malformation. In: Human Genetics. 2007 ; Vol. 122, No. 5.
@article{6cb3bb229d7a4b24b767ddf588569dc5,
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 = "12",
day = "1",
language = "English",
volume = "122",
journal = "Human Genetics",
issn = "0340-6717",
publisher = "Springer-Verlag London Ltd.",
number = "5",

}

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.

Novel human pathological mutations. Gene symbol : KRIT1. Disease: cerebral cavernous malformation. / Limaye, Nisha; 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.; Wieczorek, D.; Wood, N. W.; Boon, L.; Vikkula, M.

In: Human Genetics, Vol. 122, No. 5, 01.12.2007.

Research output: Contribution to journalArticleResearchpeer-review

TY - JOUR

T1 - Novel human pathological mutations. Gene symbol

T2 - 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 - 2007/12/1

Y1 - 2007/12/1

UR - http://www.scopus.com/inward/record.url?scp=42049096142&partnerID=8YFLogxK

M3 - Article

VL - 122

JO - Human Genetics

JF - Human Genetics

SN - 0340-6717

IS - 5

ER -

Limaye N, Revencu N, Van Regemorter N, Garzon M, Bonduelle M, Chung W et al. Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation. Human Genetics. 2007 Dec 1;122(5).