Mediterranean regions the most common b-tha-lassemia mutations are due to point mutations in gene regions that are critical for production of mRNA, such as [IVS-I-nt1 (GÆA), IVS-I-nt6 (TÆC), IVS-I-nt110 (GÆA)] which interrupt normal RNA process-ing or nonsense mutations [CD39 (CÆT)] which interrupt the translation of mRNA. The frameshift mutation CD8/9 (+G) is a very common allele in Asian Indians but is rare in the Mediterranean regions in which isolated alleles with this mutation have bee
Introduction: β –Thalassaemia was first explained by Thomas Cooly as Cooly’s anaemia in 1925. The β-...
?-Thalassemia (?-thal) is present in 59% and 75% of patients with abnormal hemoglobin disorders in n...
?-Globin haplotypes have been used to investigate the origin and spread of ?-globin mutations such a...
We have detected, for the first time in Spain, a beta degrees thalassemia caused by the mutation IVS...
We characterized the genetic nature of beta-thalassaemia in northern Portugal. Of the 164 patients s...
In this study we have carried out alpha- and beta-globin gene analysis and defined the beta-globin g...
<div><p>ABSTRACT Introduction: Beta-thalassemia is caused by a deficient synthesis of the ß-chain o...
The molecular basis of beta-thalassemia was investigated at the DNA level in 28 Belgians from 14 unr...
Background: Analyses of the genomic variation in the western Mediterranean population are being used...
Thalassemia is one of the most common single gene disorders worldwide. Nearly 80 to 90 million with ...
PubMedID: 1483699We have analyzed the ß-thalassemia mutations in 99 chromosomes of 49 adults with ß-...
The β-thalassaemias are a heterogeneous group of inherited disorders of haemoglobin synthesis, all c...
B-thalassemia is mainly caused by point mutation of B-gene. There are more than 130 mutations, while...
Beta-thalassemia is one of the most common genetic disorders in Turkey as well as in several other M...
A new frameshift mutation due to an insertion of G between codon 14/1 5 of the $-globin gene was fou...
Introduction: β –Thalassaemia was first explained by Thomas Cooly as Cooly’s anaemia in 1925. The β-...
?-Thalassemia (?-thal) is present in 59% and 75% of patients with abnormal hemoglobin disorders in n...
?-Globin haplotypes have been used to investigate the origin and spread of ?-globin mutations such a...
We have detected, for the first time in Spain, a beta degrees thalassemia caused by the mutation IVS...
We characterized the genetic nature of beta-thalassaemia in northern Portugal. Of the 164 patients s...
In this study we have carried out alpha- and beta-globin gene analysis and defined the beta-globin g...
<div><p>ABSTRACT Introduction: Beta-thalassemia is caused by a deficient synthesis of the ß-chain o...
The molecular basis of beta-thalassemia was investigated at the DNA level in 28 Belgians from 14 unr...
Background: Analyses of the genomic variation in the western Mediterranean population are being used...
Thalassemia is one of the most common single gene disorders worldwide. Nearly 80 to 90 million with ...
PubMedID: 1483699We have analyzed the ß-thalassemia mutations in 99 chromosomes of 49 adults with ß-...
The β-thalassaemias are a heterogeneous group of inherited disorders of haemoglobin synthesis, all c...
B-thalassemia is mainly caused by point mutation of B-gene. There are more than 130 mutations, while...
Beta-thalassemia is one of the most common genetic disorders in Turkey as well as in several other M...
A new frameshift mutation due to an insertion of G between codon 14/1 5 of the $-globin gene was fou...
Introduction: β –Thalassaemia was first explained by Thomas Cooly as Cooly’s anaemia in 1925. The β-...
?-Thalassemia (?-thal) is present in 59% and 75% of patients with abnormal hemoglobin disorders in n...
?-Globin haplotypes have been used to investigate the origin and spread of ?-globin mutations such a...