Clinical Presentation of Congenital Heterochromia Iridis in Pakistani Patients
Heterochromia iridis is a rare genetic disorder, characterized by variation in the concentration and distribution of the melanin pigment. It is caused by mutation in genes responsible for the synthesis of melanin pigment iris of the eye. Heterochromia Iridis is inherited as a simple Mendelian trait....
Saved in:
Main Authors: | , , , , |
---|---|
Format: | Book |
Published: |
ziauddin University,
2024-10-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Internet
Connect to this object online.3rd Floor Main Library
Call Number: |
A1234.567 |
---|---|
Copy 1 | Available |