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Genomic study of nonsyndromic hearing loss in unaffected in..:
Caio Robledo D' Angioli Costa Quaio
;
Antonio Victor Campos Coelho
;
Livia Maria Silva Moura
...
https://www.frontiersin.org/articles/10.3389/fgene.2022.921324/full. , 2022
Link:
https://doi.org/10.3389/fgene.2022.921324
RT Journal T1
Genomic study of nonsyndromic hearing loss in unaffected individuals: Frequency of pathogenic and likely pathogenic variants in a Brazilian cohort of 2,097 genomes
UL https://suche.suub.uni-bremen.de/peid=base-ftdoajarticles:oai:doaj.org_article:a725ec5d20214dbdb3f344e4e8fcf56f&Exemplar=1&LAN=DE A1 Caio Robledo D' Angioli Costa Quaio A1 Antonio Victor Campos Coelho A1 Livia Maria Silva Moura A1 Rafael Lucas Muniz Guedes A1 Kelin Chen A1 Jose Ricardo Magliocco Ceroni A1 Renata Moldenhauer Minillo A1 Marcel Pinheiro Caraciolo A1 Rodrigo de Souza Reis A1 Bruna Mascaro Cordeiro de Azevedo A1 Maria Soares Nobrega A1 Anne Caroline Barbosa Teixeira A1 Matheus Martinelli Lima A1 Thamara Rayssa da Mota A1 Marina Cadena da Matta A1 Gabriela Borges Cherulli Colichio A1 Aline Lulho Roncalho A1 Ana Flavia Martinho Ferreira A1 Gabriela Pereira Campilongo A1 Eduardo Perrone A1 Luiza do Amaral Virmond A1 Carolina Araujo Moreno A1 Joana Rosa Marques Prota A1 Marina de França A1 Murilo Castro Cervato A1 Tatiana Ferreira de Almeida A1 Joao Bosco de Oliveira Filho PB Frontiers Media S.A. YR 2022 K1 nonsyndromic hearing loss K1 hearing loss K1 deafness K1 genomics K1 whole genome sequencing K1 GJB2 (C×26) gene mutations K1 Genetics K1 QH426-470 JF https://www.frontiersin.org/articles/10.3389/fgene.2022.921324/full LK http://dx.doi.org/https://doi.org/10.3389/fgene.2022.921324 DO https://doi.org/10.3389/fgene.2022.921324 SF ELIB - SuUB Bremen
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