# A Novel SNCA A30G Mutation Causes Familial Parkinsonʼs Disease

**Type:** Papers  
**Canonical URL:** https://scholariq.org/papers/a-novel-snca-a30g-mutation-causes-familial-parkinson-s-disease/

## Facts

| Field | Value |
| --- | --- |
| Author Names | Hui Liu,Christos Koros,Timo Strohäker,Claudia Schulte,Maria Bozi,Stefanos Varvaresos,Alain Ibáñez de Opakua,Athina Maria Simitsi,Anastasia Bougea,Konstantinos Voumvourakis,Matina Maniati,Sokratis G. Papageorgiou,Ann‐Kathrin Hauser,Stefan Becker,Markus Zweckstetter,Leonidas Stefanis,Thomas Gasser |
| Citations | 115 |
| DOI | 10.1002/mds.28534 |
| Fields | Medicine,Neuroscience |
| Open Access | true |
| OA Status | hybrid |
| OA URL | https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/mds.28534 |
| OpenAlex ID | https://openalex.org/W3132021332 |
| PMID | 33617693 |
| Type | article |
| Year | 2021 |

## Paper authors

- [Christos Koros](https://scholariq.org/researchers/christos-koros/)
- [Anastasia Bougea](https://scholariq.org/researchers/anastasia-bougea/)

## 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/)
- [Hereditary Neurological Disorders](https://scholariq.org/topics/hereditary-neurological-disorders/)
- [Neurological disorders and treatments](https://scholariq.org/topics/neurological-disorders-and-treatments/)

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