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Twinkle mutation in an Italian family with external progressive ophthalmoplegia and parkinsonism: A case report and an update on the state of art.
- Source :
-
Neuroscience Letters . Nov2013, Vol. 556, p1-4. 4p. - Publication Year :
- 2013
-
Abstract
- Highlights: [•] We here describe a family with two sisters and one son affected by a PEO1 mutation. [•] The sisters had a clinical parkinsonism confirmed by FP-CIT SCAN. [•] The characteristics of parkinsonisms are fully described in the paper. [•] The paper provides a short review of the phenotypes of the parkinsonisms associated to PEO1 mutation described in the literature. [Copyright &y& Elsevier]
Details
- Language :
- English
- ISSN :
- 03043940
- Volume :
- 556
- Database :
- Academic Search Index
- Journal :
- Neuroscience Letters
- Publication Type :
- Academic Journal
- Accession number :
- 92516516
- Full Text :
- https://doi.org/10.1016/j.neulet.2013.09.034