Cap disease caused by heterozygous deletion of the β-tropomyosin gene TPM2
- 1 June 2007
- journal article
- case report
- Published by Elsevier in Neuromuscular Disorders
- Vol. 17 (6) , 433-442
- https://doi.org/10.1016/j.nmd.2007.02.015
Abstract
No abstract availableKeywords
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