Werdnig-Hoffmann disease and chronic distal spinal muscular atrophy with apparent autosomal dominant inheritance. [electronic resource]

By: Contributor(s): Producer: 19921113Description: 404-7 p. digitalISSN:
  • 0364-5134
Subject(s): Online resources: In: Annals of neurology vol. 32
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Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't

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