Friedreich ataxia 1 (Q66084914)

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A Friedreich ataxia that has material basis in homozygous or compound heterozygous mutation in FXN on 9q21.1.
  • FA1
  • FRDA1
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English
Friedreich ataxia 1
A Friedreich ataxia that has material basis in homozygous or compound heterozygous mutation in FXN on 9q21.1.
  • FA1
  • FRDA1

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