ORF » Species Summary » Homo sapiens » Reactome » Defective MMAA causes methylmalonic aciduria type cblA
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Browse by Letter Index, Genomic Locus
2 gene
The longest variant of each gene is displayed. Click the see gene variants link to see all gene variants.
Gene Symbol | Full Name |
---|---|
MMAA | methylmalonic aciduria (cobalamin deficiency) cblA type |
MUT | methylmalonyl-CoA mutase |