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Dominant GDAP1 founder 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.
Affiliation
  • Auranen M; Molecular Neurology, Biomedicum-Helsinki, University of Helsinki, Finland.
Neurogenetics ; 14(2): 123-32, 2013 May.
Article in En | MEDLINE | ID: mdl-23456260
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Full text: 1 Database: MEDLINE Main subject: Charcot-Marie-Tooth Disease / Mutation / Nerve Tissue Proteins Type of study: Etiology_studies Limits: Adolescent / Adult / Child / Humans / Middle aged Country/Region as subject: Europa Language: En Year: 2013 Type: Article
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Full text: 1 Database: MEDLINE Main subject: Charcot-Marie-Tooth Disease / Mutation / Nerve Tissue Proteins Type of study: Etiology_studies Limits: Adolescent / Adult / Child / Humans / Middle aged Country/Region as subject: Europa Language: En Year: 2013 Type: Article