In humans,the mutation disease aniridia (cong | vedclass

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(A) Aniridia is a rare genetic disorder characterized by the complete or partial absence of the iris in the eye.It is primarily caused by a mutation i

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Dominant mutation

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(A) Aniridia is a rare genetic disorder characterized by the complete or partial absence of the iris in the eye.It is primarily caused by a mutation in the $PAX6$ gene.This condition follows an autosomal dominant pattern of inheritance,meaning that a single copy of the mutated gene is sufficient to cause the disorder.Therefore,it is classified as a dominant mutation.

In humans,the mutation disease aniridia (congenital absence of iris) occurs due to:

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