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Acta Myol 2005 Oct;24 (2): 70-3. 全文索取
Clinical and histopathological aspects of central core disease associated and non-associated with RYR1 locus.

Abstract
We analysed the clinical, histochemical, ultrastructural and genetic data of patients affected by central core disease (CCD) studied during the last 20 years. From a total series of 86 CCD-families, we have identified 46 CCD families with RYR1 mutations (16 autosomal dominant, 8 autosomal recessive, 17 sporadic cases and 5 de novo mutations). Out of the other 40 CCD families, the RyR1 gene was entirely excluded in 7 families, by cDNA sequencing or linkage analysis, indicating a genetic heterogeneity of CCD.

PMID: 16550918 [Pubmed - MEDLINE]

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