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W J Kimberling Selected Research

Connexin 26

11/2001Connexin 26 gene (GJB2) mutation modulates the severity of hearing loss associated with the 1555A-->G mitochondrial mutation.
4/2000Connexin 26: required for normal auditory function.

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W J Kimberling Research Topics

Disease

5Hearing Loss (Hearing Impairment)
06/2010 - 01/2000
1Autosomal Dominant 11 Deafness
06/2010
1type 1B Usher syndrome
06/2010
1Usher Syndromes (Usher Syndrome)
08/2002
1Autosomal Recessive 12 Deafness
08/2002
1Nonsyndromic Deafness
08/2002
1type 2A Usher syndrome
07/2001
1Retinitis Pigmentosa (Pigmentary Retinopathy)
01/2000

Drug/Important Bio-Agent (IBA)

2Myosin VIIaIBA
06/2010 - 01/2000
2Retinaldehyde (Retinal)IBA
06/2010 - 01/2008
2Connexin 26IBA
11/2001 - 04/2000
1Proteins (Proteins, Gene)FDA Link
08/2002
1Cadherins (E-Cadherin)IBA
08/2002
1Anti-Bacterial Agents (Antibiotics)IBA
11/2001
1AminoglycosidesIBA
11/2001
1DNA (Deoxyribonucleic Acid)IBA
07/2001
1ConnexinsIBA
04/2000