Unravelling the Complexity of the +33 C>G [HBB:c.-18C>G] Variant in Beta Thalassemia.

Stephanou, Coralea; Petrou, Miranda; Kountouris, Petros; Makariou, Christiana; Christou, Soteroula; Hadjigavriel, Michael; Kleanthous, Marina; Papasavva, Thessalia

Stephanou, Coralea; Petrou, Miranda; Kountouris, Petros; Makariou, Christiana; Christou, Soteroula; Hadjigavriel, Michael; Kleanthous, Marina; Papasavva, Thessalia.

Afiliação

Stephanou C; Molecular Genetics Thalassemia Department, The Cyprus Institute of Neurology and Genetics, Nicosia 2371, Cyprus.
Petrou M; Molecular Genetics Thalassemia Department, The Cyprus Institute of Neurology and Genetics, Nicosia 2371, Cyprus.
Kountouris P; Molecular Genetics Thalassemia Department, The Cyprus Institute of Neurology and Genetics, Nicosia 2371, Cyprus.
Makariou C; Thalassemia Clinic Nicosia, Archbishop Makarios III Hospital, Nicosia 2012, Cyprus.
Christou S; Thalassemia Clinic Nicosia, Archbishop Makarios III Hospital, Nicosia 2012, Cyprus.
Hadjigavriel M; Thalassemia Clinic Limassol, Limassol General Hospital, Limassol 4131, Cyprus.
Kleanthous M; Molecular Genetics Thalassemia Department, The Cyprus Institute of Neurology and Genetics, Nicosia 2371, Cyprus.
Papasavva T; Molecular Genetics Thalassemia Department, The Cyprus Institute of Neurology and Genetics, Nicosia 2371, Cyprus.

Biomedicines ; 12(2)2024 Jan 27.

Article em En | MEDLINE | ID: mdl-38397898

Palavras-chave

5'UTR; HBB; genotype/phenotype correlation; silent variant; ß-thalassemia intermedia

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Biomedicines Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Chipre

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