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The molecular basis of 3-methylcrotonylglycinuria, a disorder of leucine catabolism.
Am J Hum Genet. 2001 Feb;68(2):334-46. doi: 10.1086/318202. Epub 2001 Jan 17.
Am J Hum Genet. 2001.
PMID: 11170888
Free PMC article.
The molecular basis of human 3-methylcrotonyl-CoA carboxylase deficiency.
Baumgartner MR, Almashanu S, Suormala T, Obie C, Cole RN, Packman S, Baumgartner ER, Valle D.
Baumgartner MR, et al.
J Clin Invest. 2001 Feb;107(4):495-504. doi: 10.1172/JCI11948.
J Clin Invest. 2001.
PMID: 11181649
Free PMC article.
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Human biotin-containing subunit of 3-methylcrotonyl-CoA carboxylase gene (MCCA): cDNA sequence, genomic organization, localization to chromosomal band 3q27, and expression.
Obata K, Fukuda T, Morishita R, Abe S, Asakawa S, Yamaguchi S, Yoshino M, Ihara K, Murayama K, Shigemoto K, Shimizu N, Kondo I.
Obata K, et al.
Genomics. 2001 Mar 1;72(2):145-52. doi: 10.1006/geno.2000.6366.
Genomics. 2001.
PMID: 11401427
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