PARK3

PARK3
Identifiers
AliasesPARK3, PARK3 (gene), Parkinson disease 3 (autosomal dominant, Lewy body)
External IDsGeneCards: PARK3
Orthologs
SpeciesHumanMouse
Entrez

5072

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Ensembl

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UniProt

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RefSeq (mRNA)

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RefSeq (protein)

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Location (UCSC)n/an/a
PubMed search[1]n/a
Wikidata
View/Edit Human

Parkinson disease 3 (autosomal dominant, Lewy body) is a protein that in humans is encoded by the PARK3 gene.[2]

References

  1. ↑ "Human PubMed Reference:".
  2. ↑ "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.
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