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May 22, 2000Human Molecular GeneticsOpen Access

Identification of mutations in the gene encoding lamins A/C in autosomal dominant limb girdle muscular dystrophy with atrioventricular conduction disturbances (LGMD1B)

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AMAntoine MuchirGeneral Cardiology

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Antoine Muchir (2000) studied this question.

synapsesocial.com/papers/69f53eb2e0fbb6efbd203780https://doi.org/10.1093/hmg/9.9.1453
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Also Consider

Synapse has enriched 2 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Lamin A/C Gene Mutation Associated With Dilated Cardiomyopathy With Variable Skeletal Muscle Involvement2000 · 324 citations
  2. 2Loss of a-Type Lamin Expression Compromises Nuclear Envelope Integrity Leading to Muscular Dystrophy1999 · 1,236 citations