Identification of ATP1A3 Mutations by Exome Sequencing as the Cause of Alternating Hemiplegia of Childhood in Japanese Patients

Overview of attention for article published in PLOS ONE, February 2013

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Nueva investigación de un grupo de cientificos japoneses en el que se identifican mutaciones del gen ATP1A3 como causante de…

http://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0056120 Part of this research team traveled to Brussels and…

Un'altra ricerca, effettuata da un gruppo di ricercatori e medici giapponesi con il supporto dell'associazione di famiglie AHC…

PLOS ONE: an inclusive, peer-reviewed, open-access resource from the PUBLIC LIBRARY OF SCIENCE. Reports of well-performed…