A significant number of mutations in the HBB gene that cause human b@thalassemia occur within introns or in upstream noncoding sequences. Explain why mutations in these regions often lead to severe disease, although they may not directly alter the coding regions of the gene.

Human Anatomy & Physiology (11th Edition)
11th Edition
ISBN:9780134580999
Author:Elaine N. Marieb, Katja N. Hoehn
Publisher:Elaine N. Marieb, Katja N. Hoehn
Chapter1: The Human Body: An Orientation
Section: Chapter Questions
Problem 1RQ: The correct sequence of levels forming the structural hierarchy is A. (a) organ, organ system,...
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A significant number of mutations in the HBB gene that cause
human b@thalassemia occur within introns or in upstream noncoding
sequences. Explain why mutations in these regions often
lead to severe disease, although they may not directly alter the
coding regions of the gene.

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