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What Is Mendelian disorders in humans - Thalassemia?

Thalassemia is a Mendelian disorder caused by mutations in the genes responsible for hemoglobin production, leading to anemia.

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Key Points to Remember in Mendelian disorders in humans - Thalassemia

It can be classified into alpha and beta thalassemia based on the affected globin chain.

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Mendelian disorders in humans - Thalassemia in NEET Zoology: What to Focus On

NEET may include questions on genetic inheritance patterns and the implications of such disorders.