Huntington disease-like phenotype in a patient with ANO3 mutation

Autor:	Koya Kutty, Shahedah, Mulroy, Eoin, Magrinelli, Francesca, Di Lazzaro, Giulia, Latorre, Anna, Bhatia, Kailash P.
Zdroj:	In Parkinsonism and Related Disorders September 2021 90:120-122
Databáze:	ScienceDirect
Externí odkaz:	Full Text from ScienceDirect