A new mutation of the lamin A/C gene leading to autosomal dominant axonal neuropathy, muscular dystrophy, cardiac disease, and leuconychia.

C Goizet
Journal of Medical Genetics. 2004-03-01; 41(3): 29e-29
DOI: 10.1136/jmg.2003.013383

PubMed

1. J Med Genet. 2004 Mar;41(3):e29.

A new mutation of the lamin A/C gene leading to autosomal dominant axonal
neuropathy, muscular dystrophy, cardiac disease, and leuconychia.

Goizet C, Yaou RB, Demay L, Richard P, Bouillot S, Rouanet M, Hermosilla E, Le
Masson G, Lagueny A, Bonne G, Ferrer X.

DOI: 10.1136/jmg.2003.013383
PMCID: PMC1735710
PMID: 14985400 [Indexed for MEDLINE]