Two variants of hemoglobin D in the algerian population: Hemoglobin D ouled rabah β19 (B1) Asn → Lys and hemoglobin D Iran β22 (B4) Glu → Gln-Reference-Cited by-同舟云学术

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Two variants of hemoglobin D in the algerian population: Hemoglobin D ouled rabah β19 (B1) Asn → Lys and hemoglobin D Iran β22 (B4) Glu → Gln

Published:1973-06 Issue:2 Volume:310 Page:360-364
ISSN:0005-2795
Container-title:Biochimica et Biophysica Acta (BBA) - Protein Structure
language:en
Short-container-title:Biochimica et Biophysica Acta (BBA) - Protein Structure

Author:

Elion J.,Belkhodja O.,Wajcman H.,Labie D.

Publisher

Elsevier BV

Subject

Biochemistry, Genetics and Molecular Biology (miscellaneous)

Reference13 articles.

1. Haemoglobin D Iran: β222 Glutamic Acid→Glutamine (B4)

2. Abnormal human haemoglobins

3. Fibrinogen Detroit—a Molecular Defect in the N-terminal Disulphide Knot of Human Fibrinogen?

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1. Hemoglobin variants in Muslim community in South Gujarat, Western India;International Journal of Laboratory Hematology;2013-06-25

2. Hemoglobinopathies in North Africa: A Review;Hemoglobin;2010-01

3. The significance of the hemoglobin A2 value in screening for hemoglobinopathies;Clinical Biochemistry;2009-12

4. An Infant With Homozygous Hemoglobin D-Iran;Journal of Pediatric Hematology/Oncology;2001-01

5. Hemoglobin D Trait with Alpha Thalassemia in a Saudi Family;Annals of Saudi Medicine;2000-05

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