A De Novo Mutation inTEAD1Causes Non–X-Linked Aicardi Syndrome-Reference-Cited by-同舟云学术

A De Novo Mutation inTEAD1Causes Non–X-Linked Aicardi Syndrome

Published:2015-06-19 Issue:6 Volume:56 Page:3896
ISSN:1552-5783
Container-title:Investigative Opthalmology & Visual Science
language:en
Short-container-title:Invest. Ophthalmol. Vis. Sci.

Author:

Schrauwen Isabelle¹,Szelinger Szabolcs²,Siniard Ashley L.²,Corneveaux Jason J.²,Kurdoglu Ahmet²,Richholt Ryan²,De Both Matt²,Malenica Ivana²,Swaminathan Shanker²,Rangasamy Sampathkumar²,Kulkarni Neil³,Bernes Saunder³,Buchhalter Jeffrey⁴,Ramsey Keri²,Craig David W.²,Narayanan Vinodh²,Huentelman Matthew J.²

Affiliation:

1. Dorrance Center for Rare Childhood Disorders, Translational Genomics Research Institute, Phoenix, Arizona, United States 2Neurogenomics Division, Translational Genomics Research Institute, Phoenix, Arizona, United States 3Department of Medical Genetics, U

2. Dorrance Center for Rare Childhood Disorders, Translational Genomics Research Institute, Phoenix, Arizona, United States 2Neurogenomics Division, Translational Genomics Research Institute, Phoenix, Arizona, United States

3. Phoenix Children's Hospital, Phoenix, Arizona, United States

4. Alberta Children's Hospital, University of Calgary, Alberta, Canada

Publisher

Association for Research in Vision and Ophthalmology (ARVO)

Subject

General Medicine

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