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Paper Details

Identification of the gene responsible for the cblA complementation group of vitamin B12-responsive methylmalonic acidemia based on analysis of prokaryotic gene arrangements.
Proc Natl Acad Sci U S A
111
2002
1.4, 2, 4-bp deletion, 8-bp insertion, AAA ATPase superfamily, ATP, ATP-binding cassette transporter, GTP, MMAA, RNA species, Vitamin B(12), amino acid, bacterial operons, cblA, cblA complementation group, cblA patient cell lines, cblH, cell lines, chromosome 4q31, cobalamin, genetic diseases, human, human genome, methionine, methionine synthase, methylmalonyl-CoA, methylmalonyl-CoA mutase, mitochondria, mitochondrial cobalamin reductase, orthologous sequences, patient, prokaryotic gene arrangements, stop codon, vitamin B(12), vitamin B12, vitamin B12-responsive methylmalonic acidemia
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