Premium
Expanding the Phenotype of Dystonia‐Deafness Syndrome Caused by ACTB Gene Mutation
Author(s) -
Freitas Julian Letícia,
Vale Thiago Cardoso,
Barsottini Orlando G.P.,
Pedroso José Luiz
Publication year - 2020
Publication title -
movement disorders clinical practice
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.754
H-Index - 18
ISSN - 2330-1619
DOI - 10.1002/mdc3.12854
Subject(s) - dystonia , phenotype , mutation , genetics , gene , medicine , neuroscience , biology
View Supplementary Video 1
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom