ATP1A3 mutation presenting as CAPOS syndrome + dystonia phenotype

Autor:	Sanjay Pandey, Anjali Chouksey
Rok vydání:	2020
Předmět:	Dystonia business.industry CAPOS syndrome medicine.disease Bioinformatics Phenotype Neurology Dystonia-Deafness Syndrome ATP1A3 Mutation (genetic algorithm) medicine Neurology (clinical) Geriatrics and Gerontology business
Zdroj:	Parkinsonism & Related Disorders. 78:192-194
ISSN:	1353-8020
DOI:	10.1016/j.parkreldis.2020.05.029
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::a1ee32346ce43be7a7fe924d9d749e64 https://doi.org/10.1016/j.parkreldis.2020.05.029 Zobrazit plný text záznamu Full Text from ScienceDirect