Mutations in FA2H in three Arab families with a clinical spectrum of neurodegeneration and hereditary spastic paraparesis. [electronic resource]

By: Contributor(s): Producer: 20160302Description: 95-7 p. digitalISSN:
  • 1399-0004
Subject(s): Online resources: In: Clinical genetics vol. 88
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Publication Type: Letter; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

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