(Q60195033)

English

distal myopathy 1

distal muscular dystrophy characterized by autosomal dominant inheritance that has material basis in mutation in the MYH7 gene on chromosome 14q11

  • MPD1
  • Laing distal myopathy
  • Gowers disease
  • Distal myopathy type 1
  • Laing early-onset distal myopathy
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