MSRB3

methionine sulfoxide reductase B3
OMIM: 613719
PanelMode of inheritanceDetails
1 panel
Component of the following Super Panels:
  • - Paediatric disorders
R-numbers: R67
Signed-off version 4.51
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
hearing loss, Deafness, autosomal recessive 74, 613718