HNRNPA1

heterogeneous nuclear ribonucleoprotein A1
OMIM: 164017
PanelMode of inheritanceDetails
1 panel
R-numbers: R58
Signed-off version 2.178
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
?Inclusion body myopathy wtih early-onset Paget disease without frontotemporal dementia type 3, OMIM:615424, Amyotrophic lateral sclerosis 20, OMIM:615426