Nondeletional α-Thalassemia (α2- IVS-1-116, A>G HBA2): An α2 Gene Point Mutation Detected in an African-American Female for the First Time

Publisher： Karger

E-ISSN： 1421-9662|132|1|22-23

ISSN： 0001-5792

Source： Acta Haematologica, Vol.132, Iss.1, 2013-12, pp. : 22-23

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Related content

α-Thalassemia in the United Arab Emirates

By  

Acta Haematologica, Vol. 100, Iss. 1, 1998-08 ,pp. : 49-53

Karger

Access to resources Recommend Favorite

Improvement in the Detection of α0- and Deletional α-Thalassemia by Real-Time PCR Combined with Dissociation Curve Analysis

By  

Acta Haematologica, Vol. 122, Iss. 1, 2009-08 ,pp. : 17-22

Karger

Access to resources Recommend Favorite

A Severe Case of Hemoglobin H Disease due to Compound Heterozygosity for Deletion of the Major α-Globin Regulatory Element (MCS-R2) and α0-Thalassemia

By  

Acta Haematologica, Vol. 138, Iss. 1, 2017-07 ,pp. : 61-64

Karger

Access to resources Recommend Favorite

Tyk2 Is Essential for IFN-α-Induced Gene Expression in Mast Cells

By  

International Archives of Allergy and Immunology, Vol. 134, Iss. 1, 2004-06 ,pp. : 25-29

Karger

Access to resources Recommend Favorite

A New Sickling Variant ‘Hb S-Wake β[(Glu6Val-Asn139 Ser)]’ Found in a Compound Heterozygote with Hb S β(Glu6Val) Coinherited with Homozygous α-Thalassemia-2: Phenotype and Molecular Characteristics

By  

Acta Haematologica, Vol. 124, Iss. 2, 2010-09 ,pp. : 120-124

Karger

Access to resources Recommend Favorite