Homozygous Mutation on the β-Globin Polyadenylation Signal in a Tunisian Patient with β-Thalassemia Intermedia and Coinheritance of Gilbert’s Syndrome

A Patient with β-Thalassemia Intermedia Secondary to Homozygosity for a Polyadenylation Signal Mutation (AATAAA > AATAGA) (HBB: C.*112A > G) on the β-Globin Gene

(2016) Yen-Chian Lim et al.   HEMOGLOBIN

Polymorphic variations influencing fetal hemoglobin levels: Association study in beta-thalassemia carriers and in normal individuals of Portuguese origin

(2015) Clara Pereira et al.   BLOOD CELLS MOLECULES AND DISEASES

Endocrine and Bone Complications inβ-Thalassemia Intermedia: Current Understanding and Treatment

(2015) Adlette Inati et al.   Biomed Research International

Role of co-inherited Gilbert syndrome on hyperbilirubinemia in Indian beta thalassemia patients

(2013) Pooja S. Dabke et al.   Hematology

Updates of the HbVar database of human hemoglobin variants and thalassemia mutations

(2013) Belinda Giardine et al.   NUCLEIC ACIDS RESEARCH

Variable haematological and clinical presentation of β-thalassaemia carriers and homozygotes with the Poly A (T→C) mutation in the Indian population

(2012) Khushnooma Italia et al.   EUROPEAN JOURNAL OF HAEMATOLOGY

Haplotype analysis of beta thalassemia patients in Western Iran

(2009) Zohreh Rahimi et al.   BLOOD CELLS MOLECULES AND DISEASES