Detection of intragenic SMN1 mutations in spinal muscular atrophy patients with a single copy of SMN1. [electronic resource]

By: Contributor(s): Producer: 20151229Description: 558-62 p. digitalISSN:
  • 1708-8283
Subject(s): Online resources: In: Journal of child neurology vol. 30
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't

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