Otud7a Knockout Mice Recapitulate Many Neurological Features of 15q13.3 Microdeletion Syndrome-Reference-Cited by-同舟云学术

Otud7a Knockout Mice Recapitulate Many Neurological Features of 15q13.3 Microdeletion Syndrome

Published:2018-02 Issue:2 Volume:102 Page:296-308
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Yin Jiani,Chen Wu,Chao Eugene S.,Soriano Sirena,Wang Li,Wang Wei,Cummock Steven E.,Tao Huifang,Pang Kaifang,Liu Zhandong,Pereira Fred A.,Samaco Rodney C.,Zoghbi Huda Y.,Xue Mingshan,Schaaf Christian P.

Funder

BCM Intellectual and Developmental Disabilities Research Center Neuroconnectivity, Neurovisualization and Neurobehavioral Cores

NIH

BCM Genetically Engineered Mouse Core

Whitehall Foundation

Citizens United for Research in Epilepsy

Joan and Stanford Alexander Family

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference27 articles.

1. A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures;Sharp;Nat. Genet.,2008

2. Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcome;van Bon;J. Med. Genet.,2009

3. A small homozygous microdeletion of 15q13.3 including the CHRNA7 gene in a girl with a spectrum of severe neurodevelopmental features;Liao;Am. J. Med. Genet. A.,2011

4. A 15q13.3 homozygous microdeletion associated with a severe neurodevelopmental disorder suggests putative functions of the TRPM1, CHRNA7, and other homozygously deleted genes;Lepichon;Am. J. Med. Genet. A.,2010

5. A small recurrent deletion within 15q13.3 is associated with a range of neurodevelopmental phenotypes;Shinawi;Nat. Genet.,2009

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