The detail information of Deafness, KLF7-related
OMIA Basic Information
Possible human homologues (MIM numbers):
Mendelian trait/disorder: unknown
Mode of inheritance: -
Considered a defect: yes
Year key mutation first reported: 2021
Species-specific name: -
Species-specific symbol: -
More detail information can see in
Associated Breeds
There are associated breeds.
Associated Gene
There are no associated genes.
References
Note: the references are listed in reverse chronological order (from the most recent year to the earliest year), and alphabetically by first author within a year.
| 2021 |
Xu,F.,Shan,S.,Sommerlad,S.,Seddon,J.M.,Brenig,B.: :
A Missense Mutation in the <i>KLF7</i> Gene Is a Potential Candidate Variant for Congenital Deafness in Australian Stumpy Tail Cattle Dogs. Genes (Basel) 12:, 2021. Pubmed reference: 33805165 . DOI: 10.3390/genes12040467 . |
| 2010 |
Sommerlad,S.,McRae,AF.,McDonald,B.,Johnstone,I.,Cuttell,L.,Seddon,JM.,O'Leary,CA.: :
Congenital Sensorineural Deafness in Australian Stumpy-Tail Cattle Dogs Is an Autosomal Recessive Trait That Maps to CFA10. PLoS One 5:e13364, 2010. Pubmed reference: 20967282 . DOI: 10.1371/journal.pone.0013364 . |