Cargando…
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...
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: | |
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 |
Ejemplares similares
-
Confirmation of GRHL2 as the gene for the DFNA28 locus
por: Vona, Barbara, et al.
Publicado: (2013) -
Neural Correlates of Speech Processing in Prelingually Deafened Children and Adolescents with Cochlear Implants
por: Ortmann, Magdalene, et al.
Publicado: (2013) -
When Hearing Is Tricky: Speech Processing Strategies in Prelingually Deafened Children and Adolescents with Cochlear Implants Having Good and Poor Speech Performance
por: Ortmann, Magdalene, et al.
Publicado: (2017) -
The Many Faces of DFNB9: Relating OTOF Variants to Hearing Impairment
por: Vona, Barbara, et al.
Publicado: (2020) -
An Unusual Case of Neuralgic Amyotrophy Presenting with Bilateral Phrenic Nerve and Vocal Cord Paresis
por: Holtbernd, F., et al.
Publicado: (2011)