EFTUD2deficiency in vertebrates: Identification of a novel human mutation and generation of a zebrafish model-Reference-Cited by-同舟云学术

EFTUD2deficiency in vertebrates: Identification of a novel human mutation and generation of a zebrafish model

Published:2015-06-27 Issue:7 Volume:103 Page:630-640
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:

Deml Brett¹²,Reis Linda M.¹,Muheisen Sanaa¹,Bick David¹,Semina Elena V.¹²

Affiliation:

1. Department of Pediatrics and Children's Research Institute at the Medical College of Wisconsin and Children's Hospital of Wisconsin; Milwaukee Wisconsin

2. Department of Cell Biology, Neurobiology, and Anatomy; Medical College of Wisconsin; Milwaukee Wisconsin

Funder

National Eye Institute

Publisher

Wiley

Subject

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

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/bdra.23397/fullpdf

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5. Haploinsufficiency of SF3B4, a component of the pre-mRNA spliceosomal complex, causes Nager syndrome;Bernier;Am J Hum Genet,2012

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