Species: Hu, Mu
Applications: WB, IHC, IHC-Fr, IHC-P
Host: Rabbit Polyclonal
FUNCTION: Essential in the activity of auditory pathway neurons. DISEASE: Defects in PJVK are the cause of non-syndromic sensorineural deafness autosomal recessive type 59 (DFNB59). DFNB59 is a form of sensorineural hearing impairment with absent or severely abnormal auditory brainstem response but normal otoacoustic emissions (auditory neuropathy or auditory dys-synchrony). Auditory neuropathies result from a lesion in the area including the inner hair cells, connections between the inner hair cells and the cochlear branch of the auditory nerve, the auditory nerve itself and auditory pathways of the brainstem. MISCELLANEOUS: 'Pejvak' means 'echo' in Persian.
|Product By Gene ID
- Autosomal recessive deafness type 59 protein
- deafness, autosomal recessive 59
Pathways for Pejvakin
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