Mutations in folate transporter genes and risk for human myelomeningocele-Reference-Cited by-同舟云学术

Mutations in folate transporter genes and risk for human myelomeningocele

Published:2017-09-26 Issue:11 Volume:173 Page:2973-2984
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am J Med Genet

Author:

Findley Tina O.¹^ORCID,Tenpenny Joy C.¹,O'Byrne Michelle R.²,Morrison Alanna C.³,Hixson James E.³,Northrup Hope²⁴,Au Kit Sing²^ORCID

Affiliation:

1. Division of Neonatology; The University of Texas Health Science Center at Houston; Houston Texas

2. Division of Medical Genetics, Department of Pediatrics, McGovern Medical School; The University of Texas Health Science Center at Houston; Houston Texas

3. Department of Epidemiology, Human Genetics and Environmental Sciences, School of Public Health; The University of Texas Health Science Center at Houston; Houston Texas

4. Shriners Hospital for Children; Houston Texas

Funder

National Institutes of Health

Richard W. Mithoff Professorship Fund

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference63 articles.

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3. Deep sequencing study of the MTHFR gene to identify variants associated with myelomeningocele;Aneji;Birth Defects Research Part A, Clinical and Molecular Teratology,2012

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5. Characteristics of a spina bifida population including North American Caucasian and Hispanic individuals;Au;Birth Defects Research Part A, Clinical and Molecular Teratology,2008

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