# Low frequency of α‐synuclein mutations in familial Parkinson's disease

**Type:** Papers  
**Canonical URL:** https://scholariq.org/papers/low-frequency-of-synuclein-mutations-in-familial-parkinson-s-disease/

## Facts

| Field | Value |
| --- | --- |
| Author Names | Matthew J. Farrer,Fabienne Wavrant‐De Vrièze,Richard Crook,Lizzie Boles,Jordi Pérez‐Tur,John Hardy,William G. Johnson,John C. Steele,Demetrius M. Maraganore,Katrina Gwinn,Timothy Lynch |
| Citations | 135 |
| DOI | 10.1002/ana.410430320 |
| Fields | Biochemistry, Genetics and Molecular Biology,Medicine,Neuroscience |
| Open Access | false |
| OA Status | closed |
| OpenAlex ID | https://openalex.org/W2094823374 |
| PMID | 9506559 |
| Type | article |
| Year | 1998 |

## Paper authors

- [John C. Steele](https://scholariq.org/researchers/john-c-steele/)

## Paper journal

- [Annals of Neurology](https://scholariq.org/journals/annals-of-neurology/)

## Paper primary topic

- [Parkinson's Disease Mechanisms and Treatments](https://scholariq.org/topics/parkinson-s-disease-mechanisms-and-treatments/)

## Paper topics

- [Parkinson's Disease Mechanisms and Treatments](https://scholariq.org/topics/parkinson-s-disease-mechanisms-and-treatments/)
- [Nuclear Receptors and Signaling](https://scholariq.org/topics/nuclear-receptors-and-signaling/)
- [Genetics and Neurodevelopmental Disorders](https://scholariq.org/topics/genetics-and-neurodevelopmental-disorders/)

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Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.