« Previous
Next »
Neuromuscular Disorders
Volume 20, Issue 3
, Pages 166-173
, March 2010
Multi-minicore disease and atypical periodic paralysis associated with novel mutations in the skeletal muscle ryanodine receptor (RYR1) gene
To access this article, please choose from the options below
PII: S0960-8966(09)00716-0
doi: 10.1016/j.nmd.2009.12.005
© 2010 Elsevier B.V. All rights reserved.
« Previous
Next »
Neuromuscular Disorders
Volume 20, Issue 3
, Pages 166-173
, March 2010
