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The R110C mutation in Notch3 causes variable clinical features in two Turkish families with CADASIL syndrome
13 auth.
Z. Uyguner,
A. Siva,
H. Kayserili,
S. Saip,
Ayse Altintas,
M. Apak,
Sait Albayram,
Nihal Isik,
G. Akman‐Demir,
M. Taşyürekli,
...
B. Öz,
Bernd Wollnik,
Bernd Wollnik
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4 |
2006 |
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