A novel 2q37 microdeletion containing human neural progenitors genes includingSTK25results in severe developmental delay, epilepsy, and microcephaly-Reference-Cited by-同舟云学术

A novel 2q37 microdeletion containing human neural progenitors genes includingSTK25results in severe developmental delay, epilepsy, and microcephaly

Published:2015-08-04 Issue:11 Volume:167 Page:2808-2816
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Imitola Jaime¹,Khurana Divya S.²,Teplyuk Nadiya M.³,Zucker Mark¹,Jethva Reena²,Legido Agustin²,Krichevsky Ana M.³,Frangieh Michael¹,Walsh Christopher A.⁴,Carvalho Karen S.²

Affiliation:

1. Laboratory for Neural Stem Cells and Functional Neurogenetics; Division of Neuroimmunology and Multiple Sclerosis, Departments of Neurology and Neuroscience; The Ohio State University Wexner Medical Center; Columbus Ohio

2. Section of Pediatric Neurology; St. Christopher Hospital for Children's; Drexel University College of Medicine; Philaldelphia

3. Center for Neurologic Diseases; Brigham and Women's Hospital, Harvard Medical School, Boston; Massachusetts

4. Division of Genetics and Genomics; Manton Center for Orphan Disease Research, Howard Hughes Medical Institute, Boston Children's Hospital, Harvard Medical School, Boston; Massachusetts

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.37268/fullpdf

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