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. 2021 Sep;36(9):2199-2200.
doi: 10.1002/mds.28665. Epub 2021 Jun 22.

Potential PINK1 Founder Effect in Polynesia Causing Early-Onset Parkinson's Disease

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Potential PINK1 Founder Effect in Polynesia Causing Early-Onset Parkinson's Disease

Shilpan G Patel et al. Mov Disord. 2021 Sep.
No abstract available

Keywords: PINK1; Polynesia; dystonia; early onset Parkinson's disease; recessive genetic conditions.

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References

    1. Alcalay RN, Caccappolo E, Mejia-Santana H, et al. Frequency of known mutations in early-onset Parkinson disease: implication for genetic counseling: the consortium on risk for early onset Parkinson disease study. Arch Neurol 2010;67(9):1116-1122.
    1. Rogaeva E, Johnson J, Lang AE, et al. Analysis of the PINK1 gene in a large cohort of cases with Parkinson disease. Arch Neurol 2004;61(12):1898-1904.
    1. Steele JC, Guella I, Szu-Tu C, et al. Defining neurodegeneration on Guam by targeted genomic sequencing. Ann Neurol 2015;77(3):458-468.
    1. Tan AH, Lohmann K, Tay YW, et al. PINK1 p.Leu347Pro mutations in Malays: prevalence and illustrative cases. Parkinsonism Relat Disord 2020;79:34-39.
    1. Matisoo-Smith E. Ancient DNA and the human settlement of the Pacific: a review. J Hum Evol 2015;79:93-104.

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