In humans,the mutation disease aniridia (cong | vedclass

Name: Exam Paper Generator | JEE NEET Paper Generator | Vedclass
Brand: Vedclass
Rating: 5 (35 reviews)

Question

(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

Vedclass · Accepted Answer

Dominant mutation

Vedclass · Answer

(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:

Similar Questions

$H.J. Muller$ was awarded the Nobel Prize for:

The primary source of allelic variation is

Haploids are more useful than diploids for the study of mutations because...

The rate of appearance of new forms is linked to which of the following?

Sometimes cattle or even human beings give birth to their young ones that have extremely different sets of organs,such as limbs or the position of eyes. Comment.

Vedclass Test Series

Exam Paper Generator

Online Exam Module