G. A. Vieira-Silva

Molecular and genetic characterization of a large Brazilian cohort presenting hearing loss

Diego C. B. Mariano, R. K. Tsuji, R. Bento, 2021, Human Genetics.

A rare genomic duplication in 2p14 underlies autosomal dominant hearing loss DFNA58.

D. Jagger, J. Kitajima, S. Grasel, 2020, Human molecular genetics.

Molecular and genetic characterization of a large Brazilian cohort presenting hearing loss

Diego C. B. Mariano, R. K. Tsuji, R. Bento, 2021, Human Genetics.

New Insights into the Identity of the DFNA58 Gene

J. Kitajima, A. C. Batissoco, Karina Lezirovitz, 2022, Genes.

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).

J. Kitajima, D. Moreira, G. Kobayashi, 2023, Stem cell research.