publicações selecionadas New Insights into the Identity of the DFNA58 Gene Molecular and genetic characterization of a large Brazilian cohort presenting hearing loss Generation of four induced pluripotent stem cells lines from PBMC of the DFNA58 family members: Two hearing-impaired duplication carriers (USPi006-A e USPi007-A) and two normal-hearing noncarriers (USPi004-A and USPi005-A) Utilização de células IPS para elucidação da fisiopatologia de perda auditiva sensorioneural pós-lingual de etiologia genética A rare genomic duplication in 2p14 underlies autosomal dominant hearing loss DFNA58
