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Neuromuscular Disorders
Volume 20, Issue 3
, Pages
178-187
, March 2010
Desmin myopathy with severe cardiomyopathy in a Uruguayan family due to a codon deletion in a new location within the desmin 1A rod domain
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PII: S0960-8966(10)00002-7
doi: 10.1016/j.nmd.2010.01.001
« Previous
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Neuromuscular Disorders
Volume 20, Issue 3
, Pages
178-187
, March 2010
