A mutation in the transmembrane/luminal domain of the ryanodine receptor is associated with abnormal Ca2+ release channel function and severe central core disease-Reference-Cited by-同舟云学术

A mutation in the transmembrane/luminal domain of the ryanodine receptor is associated with abnormal Ca2+ release channel function and severe central core disease

Published:1999-03-30 Issue:7 Volume:96 Page:4164-4169
ISSN:0027-8424
Container-title:Proceedings of the National Academy of Sciences
language:en
Short-container-title:Proceedings of the National Academy of Sciences

Author:

Lynch P. J.,Tong J.,Lehane M.,Mallet A.,Giblin L.,Heffron J. J. A.,Vaughan P.,Zafra G.,MacLennan D. H.,McCarthy T. V.

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

Reference34 articles.

1. A NEW CONGENITAL NON-PROGRESSIVE MYOPATHY

2. Central Core Disease

3. Central core disease: Ultrastructure of the sarcoplasmic reticulum and T-tubules

4. Expression of cytoskeleton proteins in central core disease

5. Central-core disease and malignant hyperpyrexia.

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