Phenotypic Effect of α‐Globin Gene Numbers on Indian Sickle β‐Thalassemia Patients

BACKGROUND: Sickle cell β‐thalassemia is a compound heterozygous state of β‐thalassemia and sickle cell anemia. Patient with these conditions showed mild‐to‐severe clinical phenotype. OBJECTIVES: The objective of this study was to evaluate the effects of α‐globin gene numbers on the phenotype of sic...

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Detaylı Bibliyografya
Yayımlandı:J Clin Lab Anal
Asıl Yazarlar: Pandey, Sanjay Kumar, Pandey, Sweta, Ranjan, Ravi, Shah, Vineet, Mishra, Rahasya Mani, Sharma, Monica, Saxena, Renu
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: John Wiley and Sons Inc. 2014
Konular:
Original Articles
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC6807439/
https://ncbi.nlm.nih.gov/pubmed/24395608
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/jcla.21652
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