Polygenic risk prediction and SNCA haplotype analysis in a Latino Parkinson's disease cohort (2022)
Source: Parkinsonism & Related Disorders. Unidades: FMRP, IB
Subjects: DOENÇA DE PARKINSON, HAPLOTIPOS, GENOMAS
ABNT
LOESCH, Douglas P. et al. Polygenic risk prediction and SNCA haplotype analysis in a Latino Parkinson's disease cohort. Parkinsonism & Related Disorders, v. 102, p. 7-15, 2022Tradução . . Disponível em: https://doi.org/10.1016/j.parkreldis.2022.06.010. Acesso em: 04 maio 2026.APA
Loesch, D. P., Horimoto, A. R. V. R., Sarihan, E. I., Inca-Martinez, M., Mason, E., Cornejo-Olivas, M., et al. (2022). Polygenic risk prediction and SNCA haplotype analysis in a Latino Parkinson's disease cohort. Parkinsonism & Related Disorders, 102, 7-15. doi:10.1016/j.parkreldis.2022.06.010NLM
Loesch DP, Horimoto A R V R, Sarihan EI, Inca-Martinez M, Mason E, Cornejo-Olivas M, Torres L, Mazzetti P, Cosentino C, Sarapura-Castro E, Tumas V. Polygenic risk prediction and SNCA haplotype analysis in a Latino Parkinson's disease cohort [Internet]. Parkinsonism & Related Disorders. 2022 ; 102 7-15.[citado 2026 maio 04 ] Available from: https://doi.org/10.1016/j.parkreldis.2022.06.010Vancouver
Loesch DP, Horimoto A R V R, Sarihan EI, Inca-Martinez M, Mason E, Cornejo-Olivas M, Torres L, Mazzetti P, Cosentino C, Sarapura-Castro E, Tumas V. Polygenic risk prediction and SNCA haplotype analysis in a Latino Parkinson's disease cohort [Internet]. Parkinsonism & Related Disorders. 2022 ; 102 7-15.[citado 2026 maio 04 ] Available from: https://doi.org/10.1016/j.parkreldis.2022.06.010
