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Isotalo, P.A., Wells, G.A. and Donnelly, J.G. (2000) Neonatal and fetal methylenetetrahydrofolate reductase genetic polymorphisms: An examination of C677T and A1298C mutations. The American Journal of Human Genetics, 67, 986-990.

has been cited by the following article:

• TITLE: C677T and A1298C gene polymorphisms and sporadic early-onset Alzheimer’s disease

  AUTHORS: Leila Mansouri, Sarra Klai, Najiba Fekih-Mrissa, Nasreddine Gritli, Ridha Mrissa

  KEYWORDS: A1298C MTHFR Mutation; C677T MTHFR Mutation; Early-Onset Alzheimer

  JOURNAL NAME: Advances in Alzheimer's Disease, Vol.2 No.4, December 3, 2013

  ABSTRACT: Alzheimer’s disease (AD) is a genetically complex and heterogeneous disorder. Although the clinical manifestations and the pathological features have been well elucidated, a clear etiology of AD is still unknown to this day. In the past few decades, investigations have elucidated that both the genetic and the environmental factors are capable of causing the development of AD. We report a patient with clinically diagnosed earlyonset Alzheimer's disease, age of onset 45 years. Genetic analysis revealed two MTHFR heterozygous polymorphisms C677T and A1298C.