SNX8: A candidate gene for 7p22 cardiac malformations including tetralogy of fallot-Reference-Cited by-同舟云学术

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SNX8: A candidate gene for 7p22 cardiac malformations including tetralogy of fallot

Published:2013-12-05 Issue:2 Volume:164 Page:554-556
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Vanzo Rena J.¹,Martin Megan M.¹,Sdano Mallory R.¹,Teta Kathie²,Aggarwal Vimla³,South Sarah T.⁴⁵

Affiliation:

1. Lineagen, Inc.; 423 Wakara Way; Ste 200 Salt Lake City UT 84108 United States

2. Pediatric and Adolescent Neurodevelopmental Associates; Atlanta Georgia

3. Columbia University Medical Center; Clinical Pathology; New York New York

4. ARUP Laboratories; Salt Lake City Utah

5. University of Utah; Departments of Pediatrics and Pathology; Salt Lake City Utah

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.36242/fullpdf

Reference10 articles.

1. Sorting nexin 8 regulates endosome-to-Golgi transport;Dyve;Biochem Biophys Res Comm,2009

2. Use of array comparative genome hybridization in orofacial clefting;Gallego;J Craniofac Surg,2010

3. Functional health status in adult survivors of operative repair of tetralogy of Fallot;Hickey;Am J Cardiol,2012

4. Identification of rare recurrent copy number variants in high-risk autism families and their prevalence in a large ASD population;Matsunami;PLoS ONE,2013

5. Delineation of a less than 200 kb minimal deleted region for cardiac malformations on chromosome 7p22;Richards;Am J Med Genet Part A,2011

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4. A PX-BAR protein Mvp1/SNX8 and a dynamin-like GTPase Vps1 drive endosomal recycling;ELIFE;2021

5. A PX-BAR protein Mvp1/SNX8 and a dynamin-like GTPase Vps1 drive endosomal recycling;eLife;2021-09-15

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