CONNEXIN 26 MUTATION DETECTION

104 Ratings

Rs 10,530 Rs 7,800

26 % OFF

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.

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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.

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