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                                       Details for article 3 of 9 found articles
 
 
  Dominant GDAP1 founder mutation is a common cause of axonal Charcot-Marie-Tooth disease in Finland
 
 
Title: Dominant GDAP1 founder mutation is a common cause of axonal Charcot-Marie-Tooth disease in Finland
Author: Auranen, Mari
Ylikallio, Emil
Toppila, Jussi
Somer, Mirja
Kiuru-Enari, Sari
Tyynismaa, Henna
Appeared in: Neurogenetics
Paging: Volume 14 (2013) nr. 2 pages 123-132
Year: 2013
Contents:
Publisher: Springer-Verlag, Berlin/Heidelberg
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

                             Details for article 3 of 9 found articles
 
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