CNBP

CCHC-type zinc finger nucleic acid binding protein
OMIM: 116955
PanelMode of inheritanceDetails
1 panel
Component of the following Super Panels:
  • - Hypotonic infant
  • - Neuromuscular disorders
Signed-off version 2.1
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Myotonic dystrophy 2, OMIM:602668, Myotonic dystrophy type 2, MONDO:0011266