A de novo KCNQ2 mutation detected in non-familial benign neonatal convulsions-Reference-Cited by-同舟云学术

A de novo KCNQ2 mutation detected in non-familial benign neonatal convulsions

Published:2009-01 Issue:1 Volume:31 Page:27-33
ISSN:0387-7604
Container-title:Brain and Development
language:en
Short-container-title:Brain and Development

Author:

Ishii Atsushi,Fukuma Goryu,Uehara Akira,Miyajima Tasuku,Makita Yoshio,Hamachi Akiyo,Yasukochi Midori,Inoue Takahito,Yasumoto Sawa,Okada Motohiro,Kaneko Sunao,Mitsudome Akihisa,Hirose Shinichi

Publisher

Elsevier BV

Subject

Clinical Neurology,Developmental Neuroscience,General Medicine,Pediatrics, Perinatology, and Child Health

Reference27 articles.

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3. A novel splicing mutation in KCNQ2 in a multigenerational family with BFNC followed for 25 years;de Haan;Epilepsia,2006

4. A novel mutation in KCNQ2 gene causes benign familial neonatal convulsions in a Chinese family;Tang;J. Neurol. Sci.,2004

5. De novo KCNQ2 mutations in patients with benign neonatal seizures;Claes;Neurology,2004

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