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K Kahrizi Selected Research

Autosomal Dominant 13 Deafness

10/2005Mutation of COL11A2 causes autosomal recessive non-syndromic hearing loss at the DFNB53 locus.

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K Kahrizi Research Topics

Disease

2Hearing Loss (Hearing Impairment)
06/2010 - 10/2005
1Epilepsy (Aura)
01/2018
1Intellectual Disability (Idiocy)
01/2018
1type 1B Usher syndrome
06/2010
1Autosomal Dominant 11 Deafness
06/2010
1Autosomal Dominant 13 Deafness
10/2005
1Deafness (Deaf Mutism)
10/2005

Drug/Important Bio-Agent (IBA)

1(2-hydroxymethylcyclohexyl)acetic acid lactoneIBA
01/2018
1Hydrochloric Acid (Hydrogen Chloride)FDA Link
01/2018
1Retinaldehyde (Retinal)IBA
06/2010
1Myosin VIIaIBA
06/2010
1Collagen Type XIIBA
10/2005