A Second Case of Hb Fontainebleau [α21(B2)Ala→Pro] in an Individual with Microcytosis
Author:
Publisher
Informa UK Limited
Subject
Biochemistry, medical,Clinical Biochemistry,Genetics(clinical),Hematology
Link
http://www.tandfonline.com/doi/pdf/10.1080/03630260903061135
Reference8 articles.
1. HB Fontainebleau [α21(B2)ALA→PRO], A new Silent Mutant Hemoglobin
2. HB Auckland [α87(F8)his→ASN]: A new Mutation of the Proximal Histidine Identified by Electrospray Mass Spectrometry
3. Electrospray Ionisation Analysis of Human Fibrinogen
4. Locus assignment of human a globin mutations by selective amplification and direct sequencing
5. Hemoglobin H disease: not necessarily a benign disorder
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1. A report of Hb Fontainebleau [α21 (B2) Ala > Pro] as a result of founder effect phenomenon;Gene Reports;2020-06
2. In SilicoAnalysis of the Effects of Point Mutations on α-Globin: Implications for α-Thalassemia;Hemoglobin;2020-03-03
3. First Observation of Hemoglobin G-Waimanalo and Hemoglobin Fontainebleau Cases in the Turkish Population;Turkish Journal of Hematology;2016-02-19
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