Mutations in the COPII Vesicle Component GeneSEC24Bare Associated with Human Neural Tube Defects-Reference-Cited by-全球学者库

Mutations in the COPII Vesicle Component GeneSEC24Bare Associated with Human Neural Tube Defects

Published:2013-05-13 Issue:8 Volume:34 Page:1094-1101
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Human Mutation

Author:

Yang Xue-Yan¹,Zhou Xiang-Yu¹,Wang Qing Qing²,Li Hong³,Chen Ying³,Lei Yun-Ping¹,Ma Xiao-Hang¹,Kong Pan¹,Shi Yan¹,Jin Li¹,Zhang Ting⁴,Wang Hong-Yan¹⁵

Affiliation:

1. The State Key Laboratory of Genetic Engineering and MOE Key Laboratory of Contemporary Anthropology, School of Life Sciences; Fudan University; Shanghai People's Republic of China

2. School of Life Sciences; Shaanxi Normal University; Xi'an People's Republic of China

3. The Center for Reproduction and Genetics, Suzhou Maternal-Child Medical Center; Suzhou General Hospital; Suzhou People's Republic of China

4. The Capital Institute of Pediatrics; Beijing People's Republic of China

5. The Institutes of Biomedical Sciences; Fudan University; Shanghai People's Republic of China

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/humu.22338/fullpdf

Reference22 articles.

1. Identification and characterization of novel rare mutations in the planar cell polarity gene PRICKLE1 in human neural tube defects;Bosoi;Hum Mutat,2011

2. Neural-tube defects;Botto;N Engl J Med,1999

3. FZD6 is a novel gene for human neural tube defects;De Marco;Hum Mutat,2012

4. Genetics of human neural tube defects;Greene;Hum Mol Genet,2009

5. Mouse mutants with neural tube closure defects and their role in understanding human neural tube defects;Harris;Birth Defects Res A Clin Mol Teratol,2007

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