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Correction to: Ataxia with Ocular Apraxia Type 1 (AOA1) (APTX, W279* Mutation): Neurological, Neuropsychological, and Molecular Outlining of a Heterogenous Phenotype in Four Colombian Siblings.
Aguillon D, Vasquez D, Madrigal L, Moreno S, Hernández D, Isaza-Ruget M, Lopez JJ, Landires I, Nunez-Samudio V, Restrepo CM, Vidal OM, Vélez JI, Arcos-Holzinger M, Lopera F, Arcos-Burgos M. Aguillon D, et al. Mol Neurobiol. 2022 Jun;59(6):3859. doi: 10.1007/s12035-022-02874-8. Mol Neurobiol. 2022. PMID: 35585447 No abstract available.
Potential cognitive endophenotypes in multigenerational families: segregating ADHD from a genetic isolate.
Pineda DA, Lopera F, Puerta IC, Trujillo-Orrego N, Aguirre-Acevedo DC, Hincapié-Henao L, Arango CP, Acosta MT, Holzinger SI, Palacio JD, Pineda-Alvarez DE, Velez JI, Martinez AF, Lewis JE, Muenke M, Arcos-Burgos M. Pineda DA, et al. Atten Defic Hyperact Disord. 2011 Sep;3(3):291-9. doi: 10.1007/s12402-011-0061-3. Epub 2011 Jul 16. Atten Defic Hyperact Disord. 2011. PMID: 21779842 Free PMC article.
160 results