论文信息 - Benign SCA14 phenotype in a German patient associated with a missense mutation in exon 3 of the PRKCG gene

Benign SCA14 phenotype in a German patient associated with a missense mutation in exon 3 of the PRKCG gene

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D. Timmann | E. Gizewski | L. Arning | S. Wieczorek | Ingrid Alheite

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