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A comprehensive analysis of deletions, multiplications, and copy number variations in PARK2

OBJECTIVES: To perform a comprehensive population genetic study of PARK2. PARK2 mutations are associated with juvenile parkinsonism, Alzheimer disease, cancer, leprosy, and diabetes mellitus, yet ironically, there has been no comprehensive study of PARK2 in control subjects; and to resolve controver...

Täydet tiedot

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Bibliografiset tiedot
Päätekijät: Kay, D.M., Stevens, C.F., Hamza, T.H., Montimurro, J.S., Zabetian, C.P., Factor, S.A., Samii, A., Griffith, A., Roberts, J.W., Molho, E.S., Higgins, D.S., Gancher, S., Moses, L., Zareparsi, S., Poorkaj, P., Bird, T., Nutt, J., Schellenberg, G.D., Payami, H.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: American Academy of Neurology 2010
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC3013490/
https://ncbi.nlm.nih.gov/pubmed/20876472
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/WNL.0b013e3181f4d832
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