Mutational spectrum in eight Korean patients with 3-methylcrotonyl-CoA carboxylase deficiency.

Article Details

Citation
Copy to clipboard

Cho SY, Park HD, Lee YW, Ki CS, Lee SY, Sohn YB, Park SW, Kim SH, Ji S, Kim SJ, Choi EW, Kim CH, Ko AR, Paik KH, Lee DH, Jin DK

Mutational spectrum in eight Korean patients with 3-methylcrotonyl-CoA carboxylase deficiency.

Clin Genet. 2012 Jan;81(1):96-8. doi: 10.1111/j.1399-0004.2011.01704.x.

PubMed ID
22150417 [ View in PubMed
]
Abstract

Not Available

DrugBank Data that Cites this Article

Polypeptides
NameUniProt ID
Methylcrotonoyl-CoA carboxylase beta chain, mitochondrialQ9HCC0Details
Methylcrotonoyl-CoA carboxylase subunit alpha, mitochondrialQ96RQ3Details