ArticleJournal of neuromuscular diseases2023

A Case of Oculopharyngeal Muscular Dystrophy Caused by a Novel PABPN1 c.34G > T (p.Gly12Trp) Point Mutation without Polyalanine Expansion.

Yoshiaki Takahashi et al.PubMed ↗Full text ↗Publisher ↗

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