(Q28361131)

21 June 2017

title

Examinations of methylenetetrahydrofolate reductase C677T and A1298C mutations--and in utero viability (English)

1 reference

21 June 2017

Volcik KA

1

1 reference

21 June 2017

Blanton SH

series ordinal

2

1 reference

21 June 2017

Northrup H

series ordinal

3

1 reference

21 June 2017

language of work or name

English

0 references

publication date

1 November 2001

1 reference

American Journal of Human Genetics

21 June 2017

published in

1 reference

21 June 2017

volume

69

1 reference

21 June 2017

issue

5

1 reference

21 June 2017

page(s)

1150-1153

1 reference

Neonatal and fetal methylenetetrahydrofolate reductase genetic polymorphisms: an examination of C677T and A1298C mutations

21 June 2017

cites work

1 reference

PubMed Central

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1274361

A second genetic polymorphism in methylenetetrahydrofolate reductase (MTHFR) associated with decreased enzyme activity

29 September 2017

1 reference

PubMed Central

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1274361

A common mutation A1298C in human methylenetetrahydrofolate reductase gene: association with plasma total homocysteine and folate concentrations

2 June 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/11590551

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Methylenetetrahydrofolate reductase and spina bifida: evaluation of level of defect and maternal genotypic risk in Hispanics

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/11590551

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1086/324066

1 reference

21 June 2017

0 references

1 reference