PARK3
Parkinson disease 3 (autosomal dominant, Lewy body) is a protein that in humans is encoded by the PARK3 gene.[2]
| PARK3 | |||||||||||||||||||||||||||||||||||||||||||||||||||
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| Identifiers | |||||||||||||||||||||||||||||||||||||||||||||||||||
| Aliases | PARK3, PARK3 (gene), Parkinson disease 3 (autosomal dominant, Lewy body) | ||||||||||||||||||||||||||||||||||||||||||||||||||
| External IDs | GeneCards: PARK3 | ||||||||||||||||||||||||||||||||||||||||||||||||||
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References
- "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- "Entrez Gene: Parkinson disease 3 (autosomal dominant, Lewy body)".
Further reading
- DeStefano AL, Lew MF, Golbe LI, Mark MH, Lazzarini AM, Guttman M, et al. (May 2002). "PARK3 influences age at onset in Parkinson disease: a genome scan in the GenePD study". American Journal of Human Genetics. 70 (5): 1089–95. doi:10.1086/339814. PMC 447587. PMID 11920285.
- Sharma M, Mueller JC, Zimprich A, Lichtner P, Hofer A, Leitner P, et al. (July 2006). "The sepiapterin reductase gene region reveals association in the PARK3 locus: analysis of familial and sporadic Parkinson's disease in European populations". Journal of Medical Genetics. 43 (7): 557–62. doi:10.1136/jmg.2005.039149. PMC 2593029. PMID 16443856.
- Gasser T, Müller-Myhsok B, Wszolek ZK, Oehlmann R, Calne DB, Bonifati V, et al. (March 1998). "A susceptibility locus for Parkinson's disease maps to chromosome 2p13". Nature Genetics. 18 (3): 262–5. doi:10.1038/ng0398-262. PMID 9500549. S2CID 11700866.
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