alpha-Sarcoglycan (adhalin) deficiency: complete deficiency patients are 5% of childhood-onset dystrophin-normal muscular dystrophy and most partial deficiency patients do not have gene mutations. [electronic resource]

By: Contributor(s): Producer: 19970103Description: 30-9 p. digitalISSN:
  • 0022-510X
Subject(s): Online resources: In: Journal of the neurological sciences vol. 140
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Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.; Research Support, U.S. Gov't, P.H.S.

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