De novo mutations in ATP1A3 cause alternating hemiplegia of childhood-Reference-Cited by-同舟云学术

De novo mutations in ATP1A3 cause alternating hemiplegia of childhood

Published:2012-07-29 Issue:9 Volume:44 Page:1030-1034
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Heinzen Erin L, ,Swoboda Kathryn J,Hitomi Yuki,Gurrieri Fiorella,Nicole Sophie,de Vries Boukje,Tiziano F Danilo,Fontaine Bertrand,Walley Nicole M,Heavin Sinéad,Panagiotakaki Eleni,Fiori Stefania,Abiusi Emanuela,Di Pietro Lorena,Sweney Matthew T,Newcomb Tara M,Viollet Louis,Huff Chad,Jorde Lynn B,Reyna Sandra P,Murphy Kelley J,Shianna Kevin V,Gumbs Curtis E,Little Latasha,Silver Kenneth,Ptáček Louis J,Haan Joost,Ferrari Michel D,Bye Ann M,Herkes Geoffrey K,Whitelaw Charlotte M,Webb David,Lynch Bryan J,Uldall Peter,King Mary D,Scheffer Ingrid E,Neri Giovanni,Arzimanoglou Alexis,van den Maagdenberg Arn M J M,Sisodiya Sanjay M,Mikati Mohamad A,Goldstein David B, ,

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng.2358.pdf

Reference29 articles.

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3. Mikati, M.A., Kramer, U., Zupanc, M.L. & Shanahan, R.J. Alternating hemiplegia of childhood: clinical manifestations and long-term outcome. Pediatr. Neurol. 23, 134–141 (2000).

4. Sweney, M.T. et al. Alternating hemiplegia of childhood: early characteristics and evolution of a neurodevelopmental syndrome. Pediatrics 123, e534–e541 (2009).

5. Panagiotakaki, E. et al. Evidence of a non-progressive course of alternating hemiplegia of childhood: study of a large cohort of children and adults. Brain 133, 3598–3610 (2010).

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