Lack of response to quinidine in KCNT1 -related neonatal epilepsy-Reference-Cited by-同舟云学术

Lack of response to quinidine in KCNT1 -related neonatal epilepsy

Published:2018-09-04 Issue:10 Volume:59 Page:1889-1898
ISSN:0013-9580
Container-title:Epilepsia
language:en
Short-container-title:Epilepsia

Author:

Numis Adam L.¹²,Nair Umesh³,Datta Anita N.⁴,Sands Tristan T.⁵,Oldham Michael S.¹,Patel Akash²,Li Melody³,Gazina Elena³,Petrou Steven³,Cilio Maria Roberta¹²⁶

Affiliation:

1. Department of Neurology; University of California San Francisco; San Francisco California

2. Department of Pediatrics; University of California San Francisco; San Francisco California

3. The Florey Institute of Neuroscience & Mental Health; Parkville Victoria Australia

4. Department of Pediatrics; University of British Columbia; Vancouver British Columbia Canada

5. Department of Neurology; Columbia University; New York New York

6. Institute of Human Genetics; University of California San Francisco; San Francisco California

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/epi.14551/fullpdf

Reference35 articles.

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3. De novo gain-of-function KCNT1 channel mutations cause malignant migrating partial seizures of infancy;Barcia;Nat Genet,2012

4. Formation of intermediate-conductance calcium-activated potassium channels by interaction of Slack and Slo subunits;Joiner;Nat Neurosci,1998

5. Na+-activated K+ channels express a large delayed outward current in neurons during normal physiology;Budelli;Nat Neurosci,2009

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