1 Matching Annotations
- Dec 2022
-
pubmed.ncbi.nlm.nih.gov pubmed.ncbi.nlm.nih.gov
-
Inborn errors of creatine metabolism and epilepsy: clinical features, diagnosis, and treatment
PMID: 12597058
Gene: GAMT
Disease:GAMT deficiency
Inheritance:Autosomal Recessive
-