Defective mRNA levels are responsible for a beta-thalassemia phenotype associated with Hb Federico II, a novel hemoglobin variant [beta-106 (G8) Leu->Val]

Saved in:
Bibliographic Details
Published in:Haematologica (Roma) 2008-07, Vol.93 (7), p.1096-1098
Main Authors: Grosso, Michela, Palumbo, Ilaria, Morelli, Emanuela, Puzone, Stella, Sessa, Raffaele, Izzo, Paola
Format: Article
Language:English
Subjects:
beta-Thalassemia - diagnosis
beta-Thalassemia - genetics
Codon
Female
Hemoglobins - metabolism
Hemoglobins, Abnormal - genetics
Heterozygote
Humans
Leucine - chemistry
Male
Models, Genetic
Mutation
Pedigree
Phenotype
Sequence Analysis, DNA
Valine - chemistry
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:
ISSN:0390-6078
1592-8721
DOI:10.3324/haematol.11722