WILSON DISEASE ATP7 B GENE MUTATION DETECTION
WILSON DISEASE ATP7 B GENE MUTATION DETECTION

Wilson disease is most commonly caused by mutations in the ATP7B gene. The most commonly seen mutation is H169Q,accounting for 37­63% ofmutations in Caucasians.

Sample Type - Blood

Reporting Time - Please Call Customer care

Prerequisites - No special preparation required

Price - ₹63530/-

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