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Neuromuscular Disorders
Volume 22, Issue 4
, Pages 361-367
, April 2012
A missense mutation in the skeletal muscle chloride channel 1 (CLCN1) as candidate causal mutation for congenital myotonia in a New Forest pony
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PII: S0960-8966(11)01347-2
doi: 10.1016/j.nmd.2011.10.001
© 2011 Elsevier B.V. All rights reserved.
« Previous
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Neuromuscular Disorders
Volume 22, Issue 4
, Pages 361-367
, April 2012
