ArticleMolecular neurobiology2018

Whole-Exome Sequencing Identifies a Novel Homozygous Frameshift Mutation in the MTMR2 Gene as a Causative Mutation in a Patient with Charcot-Marie-Tooth Disease Type 4B1.

Tameemi Abdalla-Moady et al.PubMed ↗Publisher ↗

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