Multi-minicore disease and atypical periodic paralysis associated with novel mutations in the skeletal muscle ryanodine receptor (RYR1) gene

Published 2010 View Full Article

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Title
Multi-minicore disease and atypical periodic paralysis associated with novel mutations in the skeletal muscle ryanodine receptor (RYR1) gene
Authors
Keywords
-
Journal
NEUROMUSCULAR DISORDERS
Volume 20, Issue 3, Pages 166-173
Publisher
Elsevier BV
Online
2010-01-19
DOI
10.1016/j.nmd.2009.12.005

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