Found: 3
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Clinical Phenotype of LRRK2 R1441C in 2 Chinese Sisters.
- Published in:
- Neurodegenerative Diseases, 2020, v. 20, n. 1, p. 39, doi. 10.1159/000508131
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- Publication type:
- Article
Clinical phenotype of Parkinson's disease with a homozygous PRKN p.Cys441Arg mutation.
- Published in:
- Neurology Asia, 2021, v. 26, n. 1, p. 161
- By:
- Publication type:
- Article
Brief Clinical Rating Scales Should Not Be Overlooked.
- Published in:
- 2020
- By:
- Publication type:
- Letter