Pages that link to "Q73041355"

The following pages link to A high-resolution genetic map around waltzer on mouse chromosome 10 and identification of a new allele of waltzer (Q73041355):

Displaying 11 items.

• Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D (Q24290695) (← links)
• Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23 (Q24535604) (← links)
• Chromosomal localization of a gene responsible for vestibulocochlear defects of BUS/Idr mice: identification as an allele of waltzer (Q28588896) (← links)
• Mutations in Cdh23, encoding a new type of cadherin, cause stereocilia disorganization in waltzer, the mouse model for Usher syndrome type 1D (Q28589238) (← links)
• A major gene affecting age-related hearing loss in C57BL/6J mice (Q28593465) (← links)
• A new mouse mutant of the Cdh23 gene with early-onset hearing loss facilitates evaluation of otoprotection drugs (Q30465306) (← links)
• The Sound of Silence: Mouse Models for Hearing Loss (Q30467805) (← links)
• Hearing loss associated with the modifier of deaf waddler (mdfw) locus corresponds with age-related hearing loss in 12 inbred strains of mice (Q30481133) (← links)
• A nuclear-mitochondrial DNA interaction affecting hearing impairment in mice (Q33821006) (← links)
• Complete exon-intron organization and chromosomal location of the gene for mouse type XIII collagen (col13a1) and comparison with its human homologue (Q33869695) (← links)
• Genomic structure, alternative splice forms and normal and mutant alleles of cadherin 23 (Cdh23). (Q43828221) (← links)