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Cobalamin deficiency
Did you mean calamine deficiency?
- ... cblB CFAP23 cob(I)alamin adenosyltransferase methylmalonic aciduria (cobalamin deficiency) cblB type methylmalonic aciduria (cobalamin deficiency) type B ...
- ... More About This Health Condition cblA methylmalonic aciduria (cobalamin deficiency) cblA type methylmalonic aciduria (cobalamin deficiency) type A methylmalonic aciduria type A MMAA_HUMAN ...
- ... About This Health Condition cblC DKFZP564I122 methylmalonic aciduria (cobalamin deficiency) cblC type, with homocystinuria methylmalonic aciduria and homocystinuria ...
- ... This Health Condition C2orf25 cblD CL25022 methylmalonic aciduria (cobalamin deficiency) cblD type, with homocystinuria methylmalonic aciduria and homocystinuria ...
- ... TCN2 gene have been found to cause transcobalamin deficiency. This condition impairs the transport of cobalamin from the bloodstream to cells throughout the body. ...
- ... Gravel RA. Molecular basis for methionine synthase reductase deficiency in patients belonging to the cblE complementation group of disorders in folate/cobalamin metabolism. Hum Mol Genet. 1999 Oct;8(11): ...
- ... NCBI Gene ClinVar ... responsiveness in biotin-responsive multiple carboxylase deficiency. Mol Genet Metab. 1999 Feb;66(2):80- ...
- ... Green R, Rosenblatt DS, Watkins D. Update on cobalamin, folate, and homocysteine. ... synthase deficiency, cblG: structure of the MTR gene, genotype diversity, ...