WRN

Werner syndrome RecQ like helicase
OMIM: 604611
PanelMode of inheritanceDetails
2 panels
Green
in Cataracts
R-numbers: R31
Signed-off version 2.76
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Werner syndrome
R-numbers: R359
Signed-off version 2.5
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Werner Syndrome, Werner syndrome, 277700