Unraveling haplotype errors in the DFNA33 locus

Genetic heterogeneity makes it difficult to identify the causal genes for hearing loss. Studies from previous decades have mapped numerous genetic loci, providing critical supporting evidence for gene discovery studies. Despite widespread sequencing accessibility, many historically mapped loci remai...

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Detalles Bibliográficos
Autores principales: Vona, Barbara, Regele, Sabrina, Rad, Aboulfazl, Strenzke, Nicola, Pater, Justin A., Neumann, Katrin, Sturm, Marc, Haack, Tobias B., Am Zehnhoff-Dinnesen, Antoinette G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10475583/
https://www.ncbi.nlm.nih.gov/pubmed/37671045
http://dx.doi.org/10.3389/fgene.2023.1214736

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10475583/
https://www.ncbi.nlm.nih.gov/pubmed/37671045
http://dx.doi.org/10.3389/fgene.2023.1214736

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