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Home Research Selected Publications Co-occurrence of the Gene ZNF9 Mutations (Myotonic Dystrophy Type 2) and Gene CLCN1 (Myotonia Congenita) in One Family - a Case Report
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Co-occurrence of the Gene ZNF9 Mutations (Myotonic Dystrophy Type 2) and Gene CLCN1 (Myotonia Congenita) in One Family - a Case Report

CESKA A SLOVENSKA NEUROLOGIE A NEUROCHIRURGIE

Parmova, O; Vohanka, S; Fajkusova, L; Stehlikova, K, 2013: Co-occurrence of the Gene ZNF9 Mutations (Myotonic Dystrophy Type 2) and Gene CLCN1 (Myotonia Congenita) in One Family - a Case Report. CESKA A SLOVENSKA NEUROLOGIE A NEUROCHIRURGIE 76(5), p. 648 - 651