Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Invitrogen
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Immunogen Sequence: KEGTHIRVNL LNHNIPKGPC ILCGMGNFKR ETVYGCFQCS VDGQKYVRLH AVPCFDIWHK RMK
Essential in the activity of auditory pathway neurons. 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. 'Pejvak' means 'echo' in Persian.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: Autosomal recessive deafness type 59 protein; DFNB59 deafness; Pejvakin
Gene Aliases: DFNB59; PJVK
UniProt ID: (Human) Q0ZLH3
Entrez Gene ID: (Human) 494513
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