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August 1, 2000Annals of Neurology

Clinical and molecular genetic spectrum of autosomal dominant Emery-Dreifuss muscular dystrophy due to mutations of the lamin A/C gene

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Authors

GBGisèle BonneHeart Failure & Transplant
Eugenio Mercuri
Eugenio MercuriUniversity of SienaAMAntoine MuchirGeneral Cardiology

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Bonne et al. (2000) studied this question.

synapsesocial.com/papers/69f53eb2e0fbb6efbd20377fhttps://doi.org/10.1002/1531-8249(200008)48:2<170::aid-ana6>3.0.co;2-j
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Also Consider

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

  1. 1Structural organization of the human gene encoding nuclear lamin A and nuclear lamin C1993 · 635 citations
  2. 2Missense Mutations in the Rod Domain of the Lamin A/C Gene as Causes of Dilated Cardiomyopathy and Conduction-System Disease1999 · 1,372 citations