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PDF-Congenital muscular dystrophies CMD are a heterogeneous group of dis

PDF-Congenital muscular dystrophies CMD are a heterogeneous group of dis

Author : elise | Published Date : 2022-09-02

WWS MEB FCMD and MDC1C are caused by mutations affecting glycosylation enzymes proteins that add sugars to other proteins In these diseases defects in the sugaradding

meb detected mutations wws detected meb wws mutations diagnosis carrier mdc1c fcmd mutation gene clinical test testing muscular individual

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Congenital muscular dystrophies CMD are a heterogeneous group of dis: Transcript

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