DominantGDAP1founder mutation is a common cause of axonal...

neurogenetics 2013 / 05 Vol. 14; Iss. 2

DominantGDAP1founder mutation is a common cause of axonal Charcot-Marie-Tooth disease in Finland

Auranen, Mari, Ylikallio, Emil, Toppila, Jussi, Somer, Mirja, Kiuru-Enari, Sari, Tyynismaa, Henna
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Volume:
14
Language:
english
Journal:
neurogenetics
DOI:
10.1007/s10048-013-0358-9
Date:
May, 2013
File:
PDF, 228 KB
english, 2013
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