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Inherited connexin mutations associated with hearing loss
Karen B. Avraham
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Corresponding author for this work
Human Molecular Genetics Biochemistry
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Keyphrases
Hearing Impairment
100%
Connexin mutation
100%
Inner Ear
66%
Gap Junction Protein
66%
Deafness
33%
Mouse Model
33%
Gap Junction
33%
Hereditary Hearing Loss
33%
Acquired Hearing Loss
33%
Connexin 26
33%
Sensory Defects
33%
Cochlear Duct
33%
Neuroscience
Gap Junction Protein
100%
Connexin 26
20%
Cochlear Duct
20%
Gap Junction
20%