| Literature DB >> 7829078 |
K A Quane1, K E Keating, J M Healy, B M Manning, R Krivosic-Horber, I Krivosic, N Monnier, J Lunardi, T V McCarthy.
Abstract
The ryanodine receptor gene (RYR1) has been shown to be mutated in a small number of malignant hyperthermia (MH) pedigrees. Missense mutations in this gene have also been identified in two families with central core disease (CCD), a rare myopathy closely associated with MH. In an effort to identify other RYR1 mutations responsible for MH and CCD, we used a SSCP approach to screen the RYR1 gene for mutations in a family exhibiting susceptibility to MH (MHS) where some of the MHS individuals display core regions in their muscle. Sequence analysis of a unique aberrant SSCP has allowed us to identify a point mutation cosegregating with MHS in the described family. The mutation changes a conserved tyrosine residue at position 522 to a serine residue. This mutation is positioned relatively close to five of the six MHS/CCD mutations known to date and provides further evidence that MHS/CCD mutations may cluster in the amino terminal region of the RYR1 protein.Entities:
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Year: 1994 PMID: 7829078 DOI: 10.1006/geno.1994.1483
Source DB: PubMed Journal: Genomics ISSN: 0888-7543 Impact factor: 5.736