Gene: [09^/IBM2] inclusion body myopathy 2, autosomal recessive;


REF

 PAT "Massa R &: Arch Neurol, 48, 519-522, 1991
LIN,LOC "Mitrani-Rosenbaum S &: Hum Mol Genet, 5, 159-163, 1996

KEY

 myo

CLA

 unknown, basic

LOC

 09 p1-q1

MIM

 MIM: 600737

Смотрите также:

  • Gene: [09^/AMCD1] arthrogryposis multiplex congenita, distal, type 1; [DA1 ]
  • Gene: [11p155/AMCD2B] arthrogryposis multiplex congenita, distal, type 2B; Freeman-Sheldon syndrome variant; [DA2B ]
  • Gene: [00.0/IBM1] inclusion body myopathy 1, autosomal dominant;