Histopathological Proof of the Pathogenetic Role of a Rare GFAP Mutation in Alexander´s Disease with Isolated Flaccid Paraparesis

Autor:	Florian Brackmann, O. Rompel, K. Rössler, Regina Trollmann, R. Coras
Rok vydání:	2017
Předmět:	Pathology medicine.medical_specialty business.industry Pediatrics Perinatology and Child Health Mutation (genetic algorithm) Medicine Neurology (clinical) General Medicine Disease business Virology
Zdroj:	Neuropediatrics. 48:S1-S45
ISSN:	1439-1899 0174-304X
DOI:	10.1055/s-0037-1602941
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::d66438b2aed320b48aabcc9f056c3055 https://doi.org/10.1055/s-0037-1602941 Zobrazit plný text záznamu