Human Methionine Synthase: cDNA Cloning and Identification of Mutations in Patients of the cblG Complementation Group of Folate/Cobalamin Disorders

By Leclerc D.   Campeau E.   Goyette P.   Adjalla C. E.   Christensen B.   Ross M.   Eydoux P.   Rosenblatt D. S.   Rozen R.   Gravel R. A.  

Human Molecular Genetics, Vol. 5, Iss. 12, 1996-12 ,pp. : 1867-1874

Oxford University Press

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Defects in Human Methionine Synthase in cblG Patients

By Gulati Sumedha   Baker Priscilla   Li Yunan N.   Fowler Brian   Kruger Warren   Brody Lawrence C.   Banerjee Ruma  

Human Molecular Genetics, Vol. 5, Iss. 12, 1996-12 ,pp. : 1859-1865

Oxford University Press

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Molecular mechanisms leading to three different phenotypes in the cblD defect of intracellular cobalamin metabolism

By Stucki Martin   Coelho David   Suormala Terttu   Burda Patricie   Fowler Brian   Baumgartner Matthias R.  

Human Molecular Genetics, Vol. 21, Iss. 6, 2012-03 ,pp. : 1410-1418

Oxford University Press

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Genetic and molecular definition of complementation group D in MHC class II deficiency

By Mach B.  

Human Molecular Genetics, Vol. 7, Iss. 5, 1998-05 ,pp. : 879-885

Oxford University Press

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Identification of the gene responsible for the cblB complementation group of vitamin B 12 -dependent methylmalonic aciduria

By Dobson C.M.  

Human Molecular Genetics, Vol. 11, Iss. 26, 2002-12 ,pp. : 3361-3369

Oxford University Press

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