PPIP5K2 and PCSK1 are Candidate Genetic Contributors to Familial Keratoconus

Keratoconus (KC) is the most common corneal ectatic disorder affecting >300,000 people in the US. KC normally has its onset in adolescence, progressively worsening through the third to fourth decades of life. KC patients report significant impaired vision-related quality of life. Genetic factors...

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Detalles Bibliográficos
Autores principales: Khaled, Mariam Lofty, Bykhovskaya, Yelena, Gu, Chunfang, Liu, Alice, Drewry, Michelle D., Chen, Zhong, Mysona, Barbara A., Parker, Emily, McNabb, Ryan P., Yu, Hongfang, Lu, Xiaowen, Wang, Jing, Li, Xiaohui, Al-Muammar, Abdulrahman, Rotter, Jerome I., Porter, Louise F., Estes, Amy, Watsky, Mitchell A., Smith, Sylvia B., Xu, Hongyan, Abu-Amero, Khaled K., Kuo, Anthony, Shears, Stephen B., Rabinowitz, Yaron S., Liu, Yutao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6920454/
https://www.ncbi.nlm.nih.gov/pubmed/31852976
http://dx.doi.org/10.1038/s41598-019-55866-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6920454/
https://www.ncbi.nlm.nih.gov/pubmed/31852976
http://dx.doi.org/10.1038/s41598-019-55866-5

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