NEETPGAI
SubjectsBlogPricing
Log inStart Free
NEETPGAI

AI-powered NEET PG preparation platform. Master all 19 subjects with adaptive MCQs, AI tutoring, and spaced repetition.

Product

  • Subjects
  • Pricing
  • Blog

Features

  • Adaptive MCQ Practice
  • AI Tutor
  • Mock Tests
  • Spaced Repetition

Resources

  • Blog
  • Study Guides
  • NEET PG Updates
  • Help Center

Legal

  • Privacy Policy
  • Terms of Service

Stay updated

© 2026 NEETPGAI. All rights reserved.
Subjects/Biochemistry/Biochemistry
Biochemistry
medium
flask-conical Biochemistry

Sickle cell anemia is a -

A. Gene deletion
B. Gene modification
C. Point mutation
D. Frame shift mutation

Explanation

Answer- c- point mutation.Sickle-cell anemia is caused by a point mutation in the b-globin chain of hemoglobin, causing the hydrophilic amino acid glutamic acid to be replaced with the hydrophobic amino acid valine at the sixth position.It is caused by a point mutation (Base substitution mutation) at the sixth position of the b-globin chain leading to subsitution of a valine residue for a glutamic acid residue resulting in sickle hemoglobin (HbS).Sickle cell anemia is an autosomal recessive disorder.

Practice similar questions

Sign up free to access AI-powered MCQ practice with detailed explanations and adaptive learning.

Start Practicing Free More Biochemistry Questions