Related content

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

Access to resources Recommend Favorite

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

Access to resources Recommend Favorite

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

Access to resources Recommend Favorite

Introducing the human Leigh syndrome mutation T9176G into Saccharomyces cerevisiae mitochondrial DNA leads to severe defects in the incorporation of Atp6p into the ATP synthase and in the mitochondrial morphology

By Kucharczyk Roza   Salin Bndicte   di Rago J.-P.  

Human Molecular Genetics, Vol. 18, Iss. 15, 2009-08 ,pp. : 2889-2898

Oxford University Press

Access to resources Recommend Favorite

The expression level of threonine synthase and cystathionine--synthase is influenced by the level of both threonine and methionine in Arabidopsis plants

By Avraham Tal  

Transgenic Research, Vol. 14, Iss. 3, 2005-06 ,pp. : 299-311

Springer Publishing Company

Access to resources Recommend Favorite