Obesity and variants of the GHRL (ghrelin) and BCHE (butyrylcholinesterase) genes

Por Dantas, Vitor G.L., Furtado-Alle, Lupe, Souza, Ricardo L.R., Chautard-Freire-Maia, Eleidi A.
Publicado em 2011

c.G2114A MYH9 mutation (DFNA17) causes non-syndromic autosomal dominant hearing loss in a Brazilian family

Por Dantas, Vitor G.L., Lezirovitz, Karina, Yamamoto, Guilherme L., Moura de Souza, Carolina Fischinger, Ferreira, Simone Gomes, Mingroni-Netto, Regina C.
Publicado no Genet Mol Biol (2014)

Characterization of a novel MYO3A missense mutation associated with a dominant form of late onset hearing loss

Por Dantas, Vitor G. L., Raval, Manmeet H., Ballesteros, Angela, Cui, Runjia, Gunther, Laura K., Yamamoto, Guilherme L., Alves, Leandro Ucela, Bueno, André Silva, Lezirovitz, Karina, Pirana, Sulene, Mendes, Beatriz C. A., Yengo, Christopher M., Kachar, Bechara, Mingroni-Netto, Regina C.
Publicado no Sci Rep (2018)