Associated Papers
Deep sequencing study of the MTHFR gene to identify variants associated with myelomeningocele.
Aneji CN et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology, 2012
The use of orthologous sequences to predict the impact of amino acid substitutions on protein function.
Marini NJ et al.
Plos Genetics, 2010
The prevalence of folate-remedial MTHFR enzyme variants in humans.
Marini NJ et al.
Proceedings of the National Academy of Sciences of the United States of America, 2008
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