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Ataxia-myoclonus syndrome due to a novel homozygous ATP13A2 mutation.
- Source :
-
Parkinsonism & related disorders [Parkinsonism Relat Disord] 2020 Jul; Vol. 76, pp. 42-43. Date of Electronic Publication: 2020 Jun 07. - Publication Year :
- 2020
- Subjects :
- Aged
Consanguinity
Humans
Male
Ataxia etiology
Ataxia genetics
Ataxia physiopathology
Myoclonus etiology
Myoclonus genetics
Myoclonus physiopathology
Parkinsonian Disorders complications
Parkinsonian Disorders diagnosis
Parkinsonian Disorders genetics
Parkinsonian Disorders physiopathology
Proton-Translocating ATPases genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1873-5126
- Volume :
- 76
- Database :
- MEDLINE
- Journal :
- Parkinsonism & related disorders
- Publication Type :
- Report
- Accession number :
- 32559632
- Full Text :
- https://doi.org/10.1016/j.parkreldis.2020.06.001