Exome sequencing reveals new causal mutations in children with epileptic encephalopathies-Reference-Cited by-同舟云学术

Exome sequencing reveals new causal mutations in children with epileptic encephalopathies

Published:2013-05-03 Issue:7 Volume:54 Page:1270-1281
ISSN:0013-9580
Container-title:Epilepsia
language:en
Short-container-title:Epilepsia

Author:

Veeramah Krishna R.¹,Johnstone Laurel¹,Karafet Tatiana M.¹,Wolf Daniel¹,Sprissler Ryan¹,Salogiannis John²,Barth-Maron Asa²,Greenberg Michael E.²,Stuhlmann Till³,Weinert Stefanie³,Jentsch Thomas J.³,Pazzi Marjorie⁴,Restifo Linda L.⁵⁶⁷,Talwar Dinesh⁴⁵⁸,Erickson Robert P.⁸⁹,Hammer Michael F.¹

Affiliation:

1. ARL Division of Biotechnology; University of Arizona; Tucson Arizona U.S.A

2. Department of Neurobiology; Harvard Medical School; Boston Massachusetts U.S.A

3. Leibniz Institute for Molecular Pharmacology (FMP) and Max-Delbrück-Center for Molecular Medicine (MDC); Berlin Germany

4. Center for Neurosciences; Tucson Arizona U.S.A

5. Department of Neurology; Arizona Health Science Center; Tucson Arizona U.S.A

6. Department of Neuroscience; University of Arizona; Tucson Arizona U.S.A

7. Department of Cellular & Molecular Medicine; Arizona Health Science Center; Tucson Arizona U.S.A

8. Department of Pediatrics; Arizona Health Science Center; Tucson Arizona U.S.A

9. Department of Molecular and Cellular Biology; University of Arizona; Tucson Arizona U.S.A

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/epi.12201/fullpdf

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