Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82

Alopecia areata is a complex genetic disease that results in hair loss due to the autoimmune-mediated attack of the hair follicle. We previously defined a role for both rare and common variants in our earlier GWAS and linkage studies. Here, we identify rare variants contributing to Alopecia Areata u...

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Detalles Bibliográficos
Autores principales: Erjavec, Stephanie O., Gelfman, Sahar, Abdelaziz, Alexa R., Lee, Eunice Y., Monga, Isha, Alkelai, Anna, Ionita-Laza, Iuliana, Petukhova, Lynn, Christiano, Angela M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8831607/
https://www.ncbi.nlm.nih.gov/pubmed/35145093
http://dx.doi.org/10.1038/s41467-022-28343-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8831607/
https://www.ncbi.nlm.nih.gov/pubmed/35145093
http://dx.doi.org/10.1038/s41467-022-28343-3

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