The Spectrum of α-Thalassemia Mutations in the Lak Population of Iran.
Iran
gene
mutation
α-Thalassemia (α-thal)
Journal
Hemoglobin
ISSN: 1532-432X
Titre abrégé: Hemoglobin
Pays: England
ID NLM: 7705865
Informations de publication
Date de publication:
Mar 2019
Mar 2019
Historique:
entrez:
16
7
2019
pubmed:
16
7
2019
medline:
14
1
2020
Statut:
ppublish
Résumé
α-Thalassemia (α-thal) is one of the most common genetic disorders worldwide. The aim of this study was to investigate for the first time the α-thal mutation spectrum in the Lak population living in Lorestan Province, Iran. One hundred and seventy-six α-thal carriers participated in the study. Multiplex gap-polymerase chain reaction (gap-PCR), amplification refractory mutation system (ARMS)-PCR and direct sequencing were used for the detection of different mutations on the α-globin (
Identifiants
pubmed: 31304855
doi: 10.1080/03630269.2019.1614049
doi:
Substances chimiques
alpha-Globins
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM