Associated Papers
Thalassemia major phenotype caused by HB Zürich-Albisrieden [α2 59(E8) Gly > Arg (HBA2:C.178G > C)] in a Brazilian child.
Pedroso GA et al.
Pediatric Blood & Cancer, 2018
Hydrops Fetalis Associated with Compound Heterozygosity for Hb Zurich-Albisrieden (HBA2: C.178G > C) and the Southeast Asian (- -SEA/) Deletion.
Yang X et al.
Hemoglobin, 2016
In-Silico Computing of the Most Deleterious nsSNPs in HBA1 Gene.
AbdulAzeez S et al.
Plos One, 2016
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