PABPN1_GCN

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Amber PABPN1_GCN STR in Limb girdle muscular dystrophies, myofibrillar myopathies and distal myopathies


Level 2: Neurology
Version 6.1
Latest signed off version: v6.0 (6 May 2026)

Component of the following Super Panels:

  • Hypotonic infant
  • Other rare neuromuscular disorders
  • review BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • Oculopharyngeal muscular dystrophy, OMIM:164300
    • oculopharyngeal muscular dystrophy, MONDO:0008116
    Tags
    • STR
    • NGS Not Validated