Finding New Genes for Non-Syndromic Hearing Loss through an In Silico Prioritization Study

At present, 51 genes are already known to be responsible for Non-Syndromic hereditary Hearing Loss (NSHL), but the knowledge of 121 NSHL-linked chromosomal regions brings to the hypothesis that a number of disease genes have still to be uncovered. To help scientists to find new NSHL genes, we built...

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Detalles Bibliográficos
Autores principales: Accetturo, Matteo, Creanza, Teresa M., Santoro, Claudia, Tria, Giancarlo, Giordano, Antonio, Battagliero, Simone, Vaccina, Antonella, Scioscia, Gaetano, Leo, Pietro
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2946934/
https://www.ncbi.nlm.nih.gov/pubmed/20927407
http://dx.doi.org/10.1371/journal.pone.0012742

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2946934/
https://www.ncbi.nlm.nih.gov/pubmed/20927407
http://dx.doi.org/10.1371/journal.pone.0012742

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