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DataSheet1_Genomic study of nonsyndromic hearing loss in un..:
Caio Robledo D' Angioli Costa Quaio
;
Antonio Victor Campos Coelho
;
Livia Maria Silva Moura
...
doi:10.3389/fgene.2022.921324.s001. , 2022
Link:
https://doi.org/10.3389/fgene.2022.921324.s001
RT Journal T1
DataSheet1_Genomic study of nonsyndromic hearing loss in unaffected individuals: Frequency of pathogenic and likely pathogenic variants in a Brazilian cohort of 2,097 genomes.xlsx
UL https://suche.suub.uni-bremen.de/peid=base-ftfrontimediafig:oai:figshare.com:article_20729059&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 Cordeiro de Mascaro A1 Maria Soares Nobrega A1 Anne Caroline Barbosa Teixeira A1 Matheus Martinelli Martinelli 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 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 YR 2022 K1 Genetics K1 Genetic Engineering K1 Biomarkers K1 Developmental Genetics (incl. Sex Determination) K1 Epigenetics (incl. Genome Methylation and Epigenomics) K1 Gene Expression (incl. Microarray and other genome-wide approaches) K1 Genome Structure and Regulation K1 Genomics K1 Genetically Modified Animals K1 Livestock Cloning K1 Gene and Molecular Therapy K1 nonsyndromic hearing loss K1 hearing loss K1 deafness K1 whole genome sequencing K1 GJB2 (C×26) gene mutations K1 STRC gene JF doi:10.3389/fgene.2022.921324.s001 LK http://dx.doi.org/https://doi.org/10.3389/fgene.2022.921324.s001 DO https://doi.org/10.3389/fgene.2022.921324.s001 SF ELIB - SuUB Bremen
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