(Q32139615)

English

megaconial type congenital muscular dystrophy

human disease

  • megaconial congenital muscular dystrophy
  • congenital megaconial myopathy
  • congenital muscular dystrophy due to phosphatidylcholine biosynthesis defect
  • congenital muscular dystrophy with mitochondrial structural abnormalities
  • MDCMC
  • Megaconial congénital muscular dystrophy
  • Muscular Dystrophy, Congenital, With Mitochondrial Structural Abnormalities
  • MUSCULAR DYSTROPHY, CONGENITAL, MEGACONIAL TYPE
  • MUSCULAR DYSTROPHY, CONGENITAL, MEGACONIAL TYPE; MDCMC

Statements

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Identifiers

 
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