Article
Mutation Update and Review of Severe Methylenetetrahydrofolate Reductase Deficiency.
Human mutation - 1 May 2016
Froese D Sean, Huemer Martina, Suormala Terttu, Burda Patricie, Coelho David, Guéant Jean-Louis, Landolt Markus A, Kožich Viktor, Fowler Brian, Baumgartner Matthias R
Abstract excerpt
Severe 5,10-methylenetetrahydrofolate reductase (MTHFR) deficiency is caused by mutations in the MTHFR gene and results in hyperhomocysteinemia and varying severity of disease, ranging from neonatal lethal to adult onset. Including those described here, 109 MTHFR mutations have been reported in 171 families, consisting of 70 missense mutations, 17 that primarily affect splicing, 11 nonsense mutations, seven small...
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