Defining novel causal SNPs and linked phenotypes at melanoma-associated loci

A number of genomic regions have been associated with melanoma risk through genome-wide association studies; however, the causal variants underlying the majority of these associations remain unknown. Here, we sequenced either the full locus or the functional regions including exons of 19 melanoma-as...

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Detalles Bibliográficos
Autores principales: Castaneda-Garcia, Carolina, Iyer, Vivek, Nsengimana, Jérémie, Trower, Adam, Droop, Alastair, Brown, Kevin M, Choi, Jiyeon, Zhang, Tongwu, Harland, Mark, Newton-Bishop, Julia A, Bishop, D Timothy, Adams, David J, Iles, Mark M, Robles-Espinoza, Carla Daniela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9433725/
https://www.ncbi.nlm.nih.gov/pubmed/35357426
http://dx.doi.org/10.1093/hmg/ddac074

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9433725/
https://www.ncbi.nlm.nih.gov/pubmed/35357426
http://dx.doi.org/10.1093/hmg/ddac074

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