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Article

Familial RYR 1 mutation associated with mild and severe central core disease.

The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques - 1 Jul 2010

Erendzhinova Ekaterina, Robinson Christopher A, Lowry Noel J, Lemire Edmond G

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 20724266
DOI: 10.1017/s031716710001060x

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Familial RYR 1 mutation associated with mild and severe central core disease.PMID 20724266Read ↗

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