Role of estrogen related receptor beta (ESRRB) in DFN35B hearing impairment and dental decay

Autor: Michael Hummel, Thottala Jayaraman, Eduardo E. Castilla, Juan C. Mereb, Dana T. Brožková, Timothy D. Ruff, Alexandre R. Vieira, José Mauro Granjeiro, Jessica Briseño-Ruiz, Hong Yuan Hsin, Mary L. Marazita, Jessalyn Forella, Marcelo de Castro Costa, Leonardo Santos Antunes, Shankar Revu, Merve Bayram, Regina C. Sencak, Erika Calvano Küchler, Megan L. Weber, Kathleen Deeley, Lívia Azeredo Alves Antunes, Vanessa M. Trombetta, Fernando A. Poletta, Hongjiao Ouyang, Patricia Nivoloni Tannure, Fernanda Volpe de Abreu, Iêda M. Orioli, Figen Seymen, Mine Koruyucu, Ersan Kalay, Takehiko Shimizu, Asli Patir

Publikováno v: BMC Medical Genetics
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET

BACKGROUND: Congenital forms of hearing impairment can be caused by mutations in the estrogen related receptor beta (ESRRB) gene. Our initial linkage studies suggested the ESRRB locus is linked to high caries experience in humans. METHODS: We tested

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a0d2c17be063fc9b616f490f9490db1
https://pubmed.ncbi.nlm.nih.gov/25023176