MTHFD1 formyltetrahydrofolate synthetase deficiency, a model for the MTHFD1 R653Q variant, leads to congenital heart defects in mice-Reference-Cited by-同舟云学术

MTHFD1 formyltetrahydrofolate synthetase deficiency, a model for the MTHFD1 R653Q variant, leads to congenital heart defects in mice

Published:2015-09-26 Issue:12 Volume:103 Page:1031-1038
ISSN:1542-0752
Container-title:Birth Defects Research Part A: Clinical and Molecular Teratology
language:en
Short-container-title:Birth Defects Research Part A: Clinical and Molecular Teratology

Author:

Christensen Karen E.¹,Deng Liyuan¹,Bahous Renata H.¹,Jerome-Majewska Loydie A.¹,Rozen Rima¹

Affiliation:

1. Departments of Human Genetics and Pediatrics; McGill University, and the Research Institute of the McGill University Health Centre; Montreal Quebec Canada

Funder

Canadian Institutes of Health Research

Publisher

Wiley

Subject

Developmental Biology,Embryology,General Medicine,Pediatrics, Perinatology, and Child Health

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/bdra.23451/fullpdf

Reference28 articles.

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2. Bates D Maechler M Bolker BM Walker S 2014 lme4: linear mixed-effects models using Eigen and S4

3. Maternal Mthfd1 disruption impairs fetal growth but does not cause neural tube defects in mice;Beaudin;Am J Clin Nutr,2012