The R110C mutation in Notch3 causes variable clinical...

Journal of the Neurological Sciences 2006 Vol. 246; Iss. 1-2

The R110C mutation in Notch3 causes variable clinical features in two Turkish families with CADASIL syndrome

Z.O. Uyguner, A. Siva, H. Kayserili, S. Saip, A. Altıntaş, M.Y. Apak, S. Albayram, N. Işık, G. Akman-Demir, M. Taşyürekli, B. Öz, B. Wollnik
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Volume:
246
Year:
2006
Language:
english
DOI:
10.1016/j.jns.2006.02.021
File:
PDF, 2.88 MB
english, 2006
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