Verpy E. et al " A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C"   Nat Genet 2000 Sep;26(1)51-55
Ahmed ZM. et al "Nonsyndromic recessive deafness DFNB18 and Usher syndrome type IC are allelic mutations of USHIC"   Hum Genet 2002 Jun;110(6)527-531
†The statements on this Web site have not been evaluated by the Food and Drug Administration (FDA). And are not intended to diagnose, treat, cure or prevent disease. The information presented is not intended to replace medical advice or treatment from your own doctor or healthcare provider. Nothing presented here is intended as a substitute for prescription medication or any other medical treatment prescribed by your doctor.