Molecular basis for methionine synthase reductase deficiency in patients belonging to the cblE complementation group of disorders in folate/cobalamin metabolism

By Wilson A.  

Human Molecular Genetics, Vol. 8, Iss. 11, 1999-10 ,pp. : 2009-2016

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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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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Cloning, Mapping and RNA Analysis of the Human Methionine Synthase Gene

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

Human Molecular Genetics, Vol. 5, Iss. 12, 1996-12 ,pp. : 1851-1858

Oxford University Press

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Human adenylosuccinate lyase (ADSL), cloning and characterization of full-length cDNA and its isoform, gene structure and molecular basis for ADSL deficiency in six patients

By Kmoch Stanislav   Hartmannová Hana   Stibùrková Blanka   Krijt Jakub   Zikánová Marie   ebesta Ivan  

Human Molecular Genetics, Vol. 9, Iss. 10, 2000-06 ,pp. : 1501-1513

Oxford University Press

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