DEPDC5 mutations in familial and sporadic focal epilepsy-Reference-Cited by-同舟云学术

DEPDC5 mutations in familial and sporadic focal epilepsy

Published:2017-03-30 Issue:4 Volume:92 Page:397-404
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clin Genet

Author:

Tsai M.-H.¹²^ORCID,Chan C.-K.³,Chang Y.-C.⁴,Yu Y.-T.¹,Chuang S.-T.¹,Fan W.-L.⁵,Li S.-C.⁶,Fu T.-Y.⁷,Chang W.-N.¹,Liou C.-W.¹,Chuang Y.-C.¹,Ng C.-C.³,Hwang D.-Y.⁸,Lim K.-S.⁹

Affiliation:

1. Department of Neurology; Kaohsiung Chang Gung Memorial Hospital; Kaohsiung Taiwan

2. Department of Nursing; Meiho University; Pingtung Taiwan

3. Genetics and Molecular Biology, Institute of Biological Sciences, Faculty of Science; University of Malaya; Kuala Lumpur Malaysia

4. Department of Pediatric Neurology; Kaohsiung Chang Gung Memorial Hospital; Kaohsiung Taiwan

5. Whole Genome Research Core Laboratory of Human Diseases; Chang Gung Medical Foundation; Keelung Taiwan

6. Genomics and Proteomics Core Laboratory, Department of Medical Research; Kaohsiung Chang Gung Memorial Hospital; Kaohsiung Taiwan

7. Department of Pathology and Laboratory Medicine; Kaohsiung Veteran General Hospital; Kaohsiung Taiwan

8. Division of Nephrology, Department of Internal Medicine; Kaohsiung Medical University Hospital, Kaohsiung Medical University; Kaohsiung Taiwan

9. Division of Neurology, Faculty of Medicine; University of Malaya; Kuala Lumpur Malaysia

Funder

Chang Gung Medical Foundation

Ministry of Science and Technology, Taiwan

Universiti Malaya

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/cge.12992/fullpdf

Reference39 articles.

1. Mutations of DEPDC5 cause autosomal dominant focal epilepsies;Ishida;Nat Genet,2013

2. Mutations in DEPDC5 cause familial focal epilepsy with variable foci;Dibbens;Nat Genet,2013

3. DEPDC5 mutations in families presenting as autosomal dominant nocturnal frontal lobe epilepsy;Picard;Neurology,2014

4. Definition and diagnostic criteria of sleep-related hypermotor epilepsy;Tinuper;Neurology,2016

5. DEPDC5 mutations are not a frequent cause of familial temporal lobe epilepsy;Striano;Epilepsia,2015

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