Abstractenetic mutations that lead to hearing losses have been identified in both human and mouse populations; the gene products include members of a class of unconventional myosins
Adult-onset hearing loss is very common, but we know little about the underlying molecular pathogen...
The identification of genes underlying monogenic, early-onset forms of deafness in humans has provid...
The identification of mutations underlying monogenic, early-onset forms of deafness in humans has pr...
Abstractenetic mutations that lead to hearing losses have been identified in both human and mouse po...
Deafness, a pathological condition causing partial or complete loss of hearing, affects nearly 70 mi...
As auditory genes and deafness-associated mutations are discovered at a rapid rate, exciting opportu...
Hearing-impaired mouse mutants not only are good models for human hereditary deafness, but also are ...
Research in the genetics of hearing and deafness has evolved rapidly over the past years, providing ...
The mammalian auditory sense organ is subdivided into three principle compartments, the outer-, midd...
The developmental and physiological complexity of the auditory system is likely reflected in the und...
The recent rapid development of molecular biology techniques applied to the genetics of normal and d...
Inherited deafness is a highly heterogeneous disorder that may be the result of mutations in any one...
International audienceAbstract Since the 1990s, the study of inherited hearing disorders, mostly tho...
The developmental and physiological complexity of the auditory system is likely reflected in the und...
Background A considerable amount of research has been published about genetic hearing impairment. Fi...
Adult-onset hearing loss is very common, but we know little about the underlying molecular pathogen...
The identification of genes underlying monogenic, early-onset forms of deafness in humans has provid...
The identification of mutations underlying monogenic, early-onset forms of deafness in humans has pr...
Abstractenetic mutations that lead to hearing losses have been identified in both human and mouse po...
Deafness, a pathological condition causing partial or complete loss of hearing, affects nearly 70 mi...
As auditory genes and deafness-associated mutations are discovered at a rapid rate, exciting opportu...
Hearing-impaired mouse mutants not only are good models for human hereditary deafness, but also are ...
Research in the genetics of hearing and deafness has evolved rapidly over the past years, providing ...
The mammalian auditory sense organ is subdivided into three principle compartments, the outer-, midd...
The developmental and physiological complexity of the auditory system is likely reflected in the und...
The recent rapid development of molecular biology techniques applied to the genetics of normal and d...
Inherited deafness is a highly heterogeneous disorder that may be the result of mutations in any one...
International audienceAbstract Since the 1990s, the study of inherited hearing disorders, mostly tho...
The developmental and physiological complexity of the auditory system is likely reflected in the und...
Background A considerable amount of research has been published about genetic hearing impairment. Fi...
Adult-onset hearing loss is very common, but we know little about the underlying molecular pathogen...
The identification of genes underlying monogenic, early-onset forms of deafness in humans has provid...
The identification of mutations underlying monogenic, early-onset forms of deafness in humans has pr...
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