KCNK9imprinting syndrome-further delineation of a possible treatable disorder-Reference-Cited by-同舟云学术

KCNK9imprinting syndrome-further delineation of a possible treatable disorder

Published:2016-05-06 Issue:10 Volume:170 Page:2632-2637
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Graham John M.¹,Zadeh Neda²,Kelley Melissa³,Tan Ee Shien⁴,Liew Wendy⁴,Tan Victoria⁴,Deardorff Matthew A.⁵⁶,Wilson Golder N.⁷⁸,Sagi-Dain Lena⁹,Shalev Stavit A.⁹¹⁰

Affiliation:

1. Department of Pediatrics; Harbor-UCLA Medical Center; Cedars-Sinai Medical Center, David Geffen School of Medicine at UCLA; Los Angeles California

2. Division of Medical Genetics; CHOC Children's Hospital; Orange California

3. KCNK9 Imprinting Syndrome Support Group; Irvine California

4. Department of Paediatric Medicine; KK Women's and Children's Hospital; Singapore

5. Department of Pediatrics; Perelman School of Medicine at the University of Pennsylvania; Philadelphia Pennsylvania

6. Division of Clinical Genetics; Children's Hospital of Philadelphia; Philadelphia Pennsylvania

7. Department of Pediatrics; Texas Tech University Health Science Center; Lubbock; Texas

8. Medical City Hospital; Dallas Texas

9. Genetic Institute; Emek Medical Center; Afula Israel

10. Rapapport Faculty of Medicine; Technion; Haifa Israel

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference9 articles.

1. Dysfunction of KCNK potassium channels impairs neuronal migration in the developing mouse cerebral cortex;Bando;Cereb Cortex,2014

2. Maternally inherited Birk Barel mental retardation dysmorphism syndrome caused by a mutation in the genomically imprinted potassium channel KCNK9;Barel;Am J Hum Genet,2008

3. Sustained high-frequency firing in cerebellar granule neurons;Brickley;J Neurosci,2007

4. Sodium and potassium channel dysfunctions in rare and common idiopathic epilepsy syndromes;Hahn;Brain Dev,2009

5. Tandem pore domain K(+)-channel TASK-3 (KCNK9) and idiopathic absence epilepsies;Kananura;Am J Med Genet,2002

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