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Copy Number Variation Analysis from SNP Genoty** Microarrays in Large Cohorts of Neurological Disorders

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  1. Article

    Correction to: Genetic Analysis of Hereditary Ataxias in Peru Identifies SCA10 Families with Incomplete Penetrance

    The original version of this article unfortunately contained some mistakes in Table 2. The additional row (just above SCA2) with the following information “SCA1, 1(1), 1, 50, 74, 24, 46 and 0/1” should be inse...

    Mario Cornejo-Olivas, Miguel Inca-Martinez, Raphael Machado Castilhos… in The Cerebellum (2020)

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  2. Article

    Open Access

    Erratum: Variable frequency of LRRK2 variants in the Latin American research consortium on the genetics of Parkinson’s disease (LARGE-PD), a case of ancestry

    A correction to this article has been published and is linked from the HTML version of this article.

    Mario Cornejo-Olivas, Luis Torres, Mario R. Velit-Salazar… in npj Parkinson's Disease (2018)

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  3. Article

    Open Access

    Variable frequency of LRRK2 variants in the Latin American research consortium on the genetics of Parkinson’s disease (LARGE-PD), a case of ancestry

    Mutations in Leucine Repeat Rich Kinase 2 (LRRK2), primarily located in codons G2019 and R1441, represent the most common genetic cause of Parkinson’s disease in European-derived populations. However, little is k...

    Mario Cornejo-Olivas, Luis Torres, Mario R. Velit-Salazar… in npj Parkinson's Disease (2017)

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  4. Article

    Open Access

    The RAB39B p.G192R mutation causes X-linked dominant Parkinson’s disease

    To identify the causal gene in a multi-incident U.S. kindred with Parkinson’s disease (PD).

    Ignacio F. Mata, Yongwoo Jang, Chun-Hyung Kim… in Molecular Neurodegeneration (2015)

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