Literature DB >> 10677336

The 1298(A-->C) mutation of methylenetetrahydrofolate reductase should be designated to the 1289 position of the gene.

J G Donnelly.   

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Year:  2000        PMID： 10677336      PMCID： PMC1288129          DOI： 10.1086/302784

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN： 0002-9297            Impact factor:   11.025


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  2 in total

Review 1.  The embryonic development of mammalian neural tube defects.

Authors:  A J Copp; F A Brook; J P Estibeiro; A S Shum; D L Cockroft
Journal:  Prog Neurobiol       Date:  1990       Impact factor: 11.685

2.  A second common mutation in the methylenetetrahydrofolate reductase gene: an additional risk factor for neural-tube defects?

Authors:  N M van der Put; F Gabreëls; E M Stevens; J A Smeitink; F J Trijbels; T K Eskes; L P van den Heuvel; H J Blom
Journal:  Am J Hum Genet       Date:  1998-05       Impact factor: 11.025
  2 in total
  2 in total

1.  Frequency of the Methylenetetrahydrofolate REDUCTASE 677CT and 1298AC mutations in an Iranian Turkish female population.

Authors:  Morteza Bagheri; Isa Abdi Rad
Journal:  Maedica (Buchar)       Date:  2010-07

2.  MTHFR C677T and A1298C polymorphisms are risk factors for Down's syndrome in Indian mothers.

Authors:  Amit Kumar Rai; Satya Singh; Stuti Mehta; Ashok Kumar; L K Pandey; Rajiva Raman
Journal:  J Hum Genet       Date:  2006-02-18       Impact factor: 3.172
  2 in total

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