Genetic etiology of Parkinson disease associated with mutations in the SNCA, PARK2, PINK1, PARK7, and LRRK2 genes: a mutation update.
- DOI
- 10.1002/humu.21277
- Published
- 2010 Jul
- Container
- Human mutation
- Publisher
- Not recorded
- Open access
- yes
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Cite this work
BibTeX
@article{allodium:10.1002/humu.21277,
title = {Genetic etiology of Parkinson disease associated with mutations in the SNCA, PARK2, PINK1, PARK7, and LRRK2 genes: a mutation update.},
author = {Nuytemans K and Theuns J and Cruts M and Van Broeckhoven C},
year = {2010},
journal = {Human mutation},
doi = {10.1002/humu.21277},
url = {https://doi.org/10.1002/humu.21277}
}RIS
TY - JOUR TI - Genetic etiology of Parkinson disease associated with mutations in the SNCA, PARK2, PINK1, PARK7, and LRRK2 genes: a mutation update. AU - Nuytemans K AU - Theuns J AU - Cruts M AU - Van Broeckhoven C PY - 2010 JO - Human mutation DO - 10.1002/humu.21277 UR - https://doi.org/10.1002/humu.21277 ER -
APA
K, N., J, T., M, C., & C, V. B. (2010). Genetic etiology of Parkinson disease associated with mutations in the SNCA, PARK2, PINK1, PARK7, and LRRK2 genes: a mutation update.. Human mutation. https://doi.org/10.1002/humu.21277
Source records
- pubmed · retrieved 2026-09-25T02:34:38.598Z