‘Absence of T378N mutation ofATP1A2gene in five patients with alternating hemiplegia of childhood’

Autor:	S Boileau, V Des Portes, Stéphane Auvin, Bernard Sablonnière, Louis Vallée, S. Marignier, Isabelle Vuillaume
Rok vydání:	2008
Předmět:	Genetics business.industry Alternating hemiplegia of childhood medicine.disease Exon Developmental Neuroscience ATP1A2 Pediatrics Perinatology and Child Health Mutation (genetic algorithm) DNA Mutational Analysis Medicine Neurology (clinical) business Gene
Zdroj:	Developmental Medicine & Child Neurology. 50:879-880
ISSN:	1469-8749 0012-1622
DOI:	10.1111/j.1469-8749.2008.03111.x
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::88b4a16e2cb959c403ba5219ebe2d7d3 https://doi.org/10.1111/j.1469-8749.2008.03111.x Zobrazit plný text záznamu Plný text