A novel GDAP1 mutation P78L responsible for CMT4A disease in three Moroccan families. [electronic resource]

By: Contributor(s): Producer: 20080123Description: 421-6 p. digitalISSN:
  • 0317-1671
Subject(s): Online resources: In: The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques vol. 34
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't

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