Expression and replication studies to identify new candidate genes involved in normal hearing function.
Considerable progress has been made in identifying deafness genes, but still little is known about the genetic basis of normal variation in hearing function. We recently carried out a Genome Wide Association Study (GWAS) of quantitative hearing traits in southern European populations and found sever...
Saved in:
| Main Authors: | Giorgia Girotto, Dragana Vuckovic, Annalisa Buniello, Beatriz Lorente-Cánovas, Morag Lewis, Paolo Gasparini, Karen P Steel |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Public Library of Science (PLoS)
2014-01-01
|
| Series: | PLoS ONE |
| Online Access: | https://doi.org/10.1371/journal.pone.0085352 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Linkage study and exome sequencing identify a BDP1 mutation associated with hereditary hearing loss.
by: Giorgia Girotto, et al.
Published: (2013-01-01) -
Correction: Expression and Replication Studies to Identify New Candidate Genes Involved in Normal Hearing Function
Published: (2014-01-01) -
Grxcr1 regulates hair bundle morphogenesis and is required for normal mechanoelectrical transduction in mouse cochlear hair cells.
by: Beatriz Lorente-Cánovas, et al.
Published: (2022-01-01) -
Wbp2 is required for normal glutamatergic synapses in the cochlea and is crucial for hearing
by: Annalisa Buniello, et al.
Published: (2016-02-01) -
Inner hair cell dysfunction in Klhl18 mutant mice leads to low frequency progressive hearing loss.
by: Neil J Ingham, et al.
Published: (2021-01-01)