Hb L'Aquila [β106(G8)Leu→Val,CTG→GTG]: A Novel Thalassemic Hemoglobin Variant-Reference-Cited by-同舟云学术

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Hb L'Aquila [β106(G8)Leu→Val,CTG→GTG]: A Novel Thalassemic Hemoglobin Variant

Published:2007-01 Issue:3 Volume:31 Page:375-378
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Amato Antonio,Pia Cappabianca Maria,Ponzini Donatella,Rinaldi Silvana,Di Biagio Paola,Foglietta Enrica,Grisanti Paola,Mastropietro Fabrizio

Publisher

Informa UK Limited

Subject

Biochemistry, medical,Clinical Biochemistry,Genetics(clinical),Hematology

Link

http://www.tandfonline.com/doi/pdf/10.1080/03630260701462055

Reference5 articles.

1. HbVar: A relational database of human hemoglobin variants and thalassemia mutations at the globin gene server

2. HB Tübingen [α2β2106(68)LEL→GLN] in a Belgian Family

3. Hemoglobin southampton (Casper): Characterization of the base mutation

4. Hemoglobin Terre Haute arginine beta 106. A posthumous correction to the original structure of hemoglobin Indianapolis.

5. The Thalassaemia Syndromes

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1. Carrier screening for inherited haemoglobin disorders among secondary school students and young adults in Latium, Italy;Journal of Community Genetics;2013-10-27

2. Prevention strategies for severe hemoglobinopathies in endemic and nonendemic immigration countries: the Latium example;Prenatal Diagnosis;2009-10-08

3. SCREENING AND GENETIC DIAGNOSIS OF HEMOGLOBINOPATHIES IN SOUTHERN AND NORTHERN EUROPE: TWO EXAMPLES;Mediterranean Journal of Hematology and Infectious Diseases;2009

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