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Article

Phenotype of a patient with recessive centronuclear myopathy and a novel BIN1 mutation.

Neurology - 9 Feb 2010

Claeys K G, Maisonobe T, Böhm J, Laporte J, Hezode M, Romero N B, Brochier G, Bitoun M, Carlier R Y, Stojkovic T

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Topics

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Share to Adaptor Proteins, Signal Transducing
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Share to BIN1 gene
Share to Myopathies, Structural, Congenital

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 20142620
DOI: 10.1212/WNL.0b013e3181cef7f9

Genes

BIN1

Provenance

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