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Identification of rare variants for hypertension with incorporation of linkage information

We conducted linkage analysis using the genome-wide association study data on chromosome 3, and then assessed association between hypertension and rare variants of genes located in the regions showing evidence of linkage. The rare variants were collapsed if their minor allele frequencies were less t...

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Detalles Bibliográficos
Autores principales: Chiu, Yen-Feng, Chung, Ren-Hua, Lee, Chun-Yi, Kao, Hui-Yi, Hou, Lin, Hsu, Fang-Chi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4144469/
https://www.ncbi.nlm.nih.gov/pubmed/25519312
http://dx.doi.org/10.1186/1753-6561-8-S1-S109

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