Limb-girdle muscular dystrophy and Miyoshi myopathy in an aboriginal Canadian kindred map to LGMD2B and segregate with the same haplotype. [electronic resource]

By: Contributor(s): Producer: 19961121Description: 872-8 p. digitalISSN:
  • 0002-9297
Subject(s): In: American journal of human genetics vol. 59
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't

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