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Results 1 - 8 of 8 for Cobalamin deficiency
Did you mean calamine deficiency?
  1. ... cblB CFAP23 cob(I)alamin adenosyltransferase methylmalonic aciduria (cobalamin deficiency) cblB type methylmalonic aciduria (cobalamin deficiency) type B ...
  2. ... More About This Health Condition cblA methylmalonic aciduria (cobalamin deficiency) cblA type methylmalonic aciduria (cobalamin deficiency) type A methylmalonic aciduria type A MMAA_HUMAN ...
  3. ... About This Health Condition cblC DKFZP564I122 methylmalonic aciduria (cobalamin deficiency) cblC type, with homocystinuria methylmalonic aciduria and homocystinuria ...
  4. ... This Health Condition C2orf25 cblD CL25022 methylmalonic aciduria (cobalamin deficiency) cblD type, with homocystinuria methylmalonic aciduria and homocystinuria ...
  5. ... TCN2 gene have been found to cause transcobalamin deficiency. This condition impairs the transport of cobalamin from the bloodstream to cells throughout the body. ...
  6. ... 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): ...
  7. ... NCBI Gene ClinVar ... responsiveness in biotin-responsive multiple carboxylase deficiency. Mol Genet Metab. 1999 Feb;66(2):80- ...
  8. ... Green R, Rosenblatt DS, Watkins D. Update on cobalamin, folate, and homocysteine. ... synthase deficiency, cblG: structure of the MTR gene, genotype diversity, ...