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Article

Exome sequencing as a diagnostic tool to identify a causal mutation in genetically highly heterogeneous limb-girdle muscular dystrophy.

Journal of human genetics - 1 Aug 2013

Matsuura Tohru, Kurosaki Tatsuaki, Omote Yoshio, Minami Narihiro, Hayashi Yukiko K, Nishino Ichizo, Abe Koji

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 23677060
DOI: 10.1038/jhg.2013.33

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