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Results 1 - 4 of 4 for chorea
  1. ... OPA3_HUMAN optic atrophy 3 (autosomal recessive, with chorea and spastic paraplegia) Tests of OPA3 PubMed OUTER ...
  2. ... the VPS13A gene have been found to cause chorea-acanthocytosis. Most of these mutations insert or delete ... are specific to single families, although people with chorea-acanthocytosis who are French-Canadian or Japanese tend ...
  3. ... novo ADCY5 mutation causes early-onset autosomal dominant chorea and dystonia. Mov Disord. 2015 Mar;30(3): ... ADCY5 mutations are another cause of benign hereditary chorea. Neurology. 2015 Jul 7;85(1):80-8. ...
  4. ... common features of this syndrome are benign hereditary chorea, which involves involuntary jerking movements (chorea) of the face, torso, and limbs and other ...