Open AccessDysarthria, ataxia, and dystonia associated with COX20 (FAM36A) gene mutation: A case report of a Turkish child
Author(s) -
Duygu G Ozcanyuz,
Faruk Incecık,
Özlem Hergüner,
Neslihan Önenli Mungan,
Sevcan Tuğ Bozdoğan
Publication year - 2020
Publication title -
annals of indian academy of neurology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.427
H-Index - 31
eISSN - 1998-3549
pISSN - 0972-2327
DOI - 10.4103/aian.aian_536_19
Subject(s) - dysarthria , medicine , dystonia , turkish , ataxia , genetics , mutation , pediatrics , gene , physical medicine and rehabilitation , audiology , psychiatry , linguistics , biology , philosophy