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De Novo Mutation in TMEM151A and Paroxysmal Kinesigenic Dyskinesia
Author(s) -
Wirth Thomas,
Méneret Aurélie,
Drouot Nathalie,
Rudolf Gabrielle,
Lagha Boukbiza Ouhaid,
Chelly Jamel,
Tranchant Christine,
Piton Amélie,
Roze Emmanuel,
Anheim Mathieu
Publication year - 2022
Publication title -
movement disorders
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 3.352
H-Index - 198
eISSN - 1531-8257
pISSN - 0885-3185
DOI - 10.1002/mds.29023
Subject(s) - missense mutation , paroxysmal dyskinesia , exome sequencing , genetics , mutation , exome , medical genetics , medicine , population , biology , gene , bioinformatics , dyskinesia , disease , environmental health , parkinson's disease
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