Type II (adult onset) Alexander disease in a paraplegic male with a rare D128N mutation in the GFAP gene. [electronic resource]

By: Contributor(s): Producer: 20160726Description: 298-302 p. digitalISSN:
  • 0722-5091
Subject(s): Online resources: In: Clinical neuropathology vol. 34
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Publication Type: Case Reports; Letter; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

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