№ files_lp_3_process_9_44221
Educational case study presenting clinical, genetic, structural, and biochemical analysis questions concerning a newborn diagnosed with a hemoglobin γ-chain V67M mutation associated with cyanosis and reported in a peer-reviewed medical journal.
Author: Shuchismita Dutta
Institution: Institute of Quantitative Biomedicine, Rutgers University, Piscataway NJ 08854
Geographic location: Toms River, New Jersey, United States
Year of case: 2008
Year of publication: 2011
Journal referenced: New England Journal of Medicine
Related article: Patch (Toms River edition)
Medical focus: Cyanosis in a newborn
Genetic focus: Hemoglobin Toms River mutation (V67M in γ-globin)
Protein studied: Fetal hemoglobin (α2γ2)
Research methods referenced: DNA sequencing, structural analysis using Protein Data Bank, laser photolysis, rapid mixing kinetics
Protein database referenced: Protein Data Bank
Structure visualization tool referenced: iCn3D
Native protein structure referenced: PDB ID 4MQJ
Biological system used: Escherichia coli expression system
Type of document: Educational case study with research analysis questions
Intended audience: Students in biochemistry, molecular biology, or biomedical sciences
Subject area: Molecular basis of cyanosis and hemoglobin mutation
Price: 8 / 10 USD
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