Unraveling haplotype errors in the DFNA33 locus

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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Bibliografske podrobnosti
Main Authors: Barbara Vona, Sabrina Regele, Aboulfazl Rad, Nicola Strenzke, Justin A. Pater, Katrin Neumann, Marc Sturm, Tobias B. Haack, Antoinette G. Am Zehnhoff-Dinnesen
Format: Article
Jezik:English
Izdano: Frontiers Media S.A. 2023-08-01
Serija:Frontiers in Genetics
Teme:
ATP11A
DFNA33
genome sequencing
haplotype analysis
hereditary hearing loss
unresolved deafness loci
Online dostop:https://www.frontiersin.org/articles/10.3389/fgene.2023.1214736/full

Internet

https://www.frontiersin.org/articles/10.3389/fgene.2023.1214736/full

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