CONNEXIN 26 (CX26) IS A PROTEIN FOUND ON THE (GJB2) GENE AND IS THE MOST COMMON CAUSE OF CONGENITAL SENSORINEURAL HEARING LOSS. CONNEXIN 26 MUTATIONS ARE RESPONSIBLE FOR AT LEAST 20% OF ALL GENETIC HEARING LOSS AND 10% OF ALL CHILDHOOD HEARING LOSS.
Why book with us?
Free and On Schedule Sample Collection
24/7 Service
Affordable
Quick and Accurate Reports
4 ML (2 ML MIN.) WHOLE BLOOD IN 1 LAVENDER TOP (EDTA) TUBE. SHIP REFRIGERATED. DO NOT FREEZE. DULY FILLED GENOMICS CLINICAL INFORMATION REQUISITION FORM IS MANDATORY.
PCR
REPORT ON 15TH DAY EVENING 7PM
DULY FILLED GENOMICS CLINICAL INFORMATION REQUISITION FORM IS MANDATORY.