A2ML1 and otitis media: novel variants, differential expression and relevant pathways

A genetic basis for otitis media is established, however the role of rare variants in disease etiology is largely unknown. Previously a duplication variant within A2ML1 was identified as a significant risk factor for otitis media in an indigenous Filipino population and in US children. In this repor...

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Publicado no:Hum Mutat
Main Authors: Larson, Eric D., Magno, Jose Pedrito M., Steritz, Matthew J., Llanes, Erasmo Gonzalo d.V., Cardwell, Jonathan, Pedro, Melquiadesa, Roberts, Tori Bootpetch, Einarsdottir, Elisabet, Rosanes, Rose Anne Q., Greenlee, Christopher, Santos, Rachel Ann P., Yousaf, Ayesha, Streubel, Sven-Olrik, Santos, Aileen Trinidad R., Ruiz, Amanda G., Lagrana-Villagracia, Sheryl Mae, Ray, Dylan, Yarza, Talitha Karisse L., Scholes, Melissa A., Anderson, Catherine B., Acharya, Anushree, Gubbels, Samuel P., Bamshad, Michael J., Cass, Stephen P., Lee, Nanette R., Shaikh, Rehan S., Nickerson, Deborah A., Mohlke, Karen L., Prager, Jeremy D., Cruz, Teresa Luisa G., Yoon, Patricia J., Abes, Generoso T., Schwartz, David A., Chan, Abner L., Wine, Todd M., Cutiongco-de la Paz, Eva Maria, Friedman, Norman, Kechris, Katerina, Kere, Juha, Leal, Suzanne M., Yang, Ivana V., Patel, Janak A., Tantoco, Ma. Leah C., Riazuddin, Saima, Chan, Kenny H., Mattila, Petri S., Reyes-Quintos, Maria Rina T., Ahmed, Zubair M., Jenkins, Herman A., Chonmaitree, Tasnee, Hafrén, Lena, Chiong, Charlotte M., Santos-Cortez, Regie Lyn P.
Formato: Artigo
Idioma:Inglês
Publicado em: 2019
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6711784/
https://ncbi.nlm.nih.gov/pubmed/31009165
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/humu.23769
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