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Comment
. 2014 May;75(5):631-3.
doi: 10.1002/ana.24160. Epub 2014 May 8.

DEPDC5 does it all: shared genetics for diverse epilepsy syndromes

Annapurna Poduri  1
Affiliations
Comment

DEPDC5 does it all: shared genetics for diverse epilepsy syndromes

Annapurna Poduri. Ann Neurol. 2014 May.
No abstract available

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  • Mutations in mammalian target of rapamycin regulator DEPDC5 cause focal epilepsy with brain malformations.
    Scheffer IE, Heron SE, Regan BM, Mandelstam S, Crompton DE, Hodgson BL, Licchetta L, Provini F, Bisulli F, Vadlamudi L, Gecz J, Connelly A, Tinuper P, Ricos MG, Berkovic SF, Dibbens LM. Scheffer IE, et al. Ann Neurol. 2014 May;75(5):782-7. doi: 10.1002/ana.24126. Epub 2014 Apr 14. Ann Neurol. 2014. PMID: 24585383
  • DEPDC5 mutations in genetic focal epilepsies of childhood.
    Lal D, Reinthaler EM, Schubert J, Muhle H, Riesch E, Kluger G, Jabbari K, Kawalia A, Bäumel C, Holthausen H, Hahn A, Feucht M, Neophytou B, Haberlandt E, Becker F, Altmüller J, Thiele H, Lemke JR, Lerche H, Nürnberg P, Sander T, Weber Y, Zimprich F, Neubauer BA. Lal D, et al. Ann Neurol. 2014 May;75(5):788-92. doi: 10.1002/ana.24127. Epub 2014 Apr 14. Ann Neurol. 2014. PMID: 24591017

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