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Article

Genotype-phenotype correlations in hereditary muscle diseases. Implications for diagnosis and treatment.

Supplements to Clinical neurophysiology - 1 Jan 2004

Leshner Robert T

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Share to Diagnosis, Differential
Share to Genetic Diseases, Inborn
Share to Laminin
Share to Muscular Diseases

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Muscular Dystrophies, Limb-Girdle

Share to Myotonic Dystrophy

Share to Pentosyltransferases

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Identifiers

PMID: 16106630
DOI: 10.1016/s1567-424x(09)70368-x

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