Setup of a Protocol of Molecular Diagnosis of β‐Thalassemia Mutations in Tunisia using Denaturing High‐Performance Liquid Chromatography (DHPLC)

BACKGROUNDS: β‐Thalassemia is one of the most prevalent worldwide autosomal recessive disorders. It presents a great molecular heterogeneity resulting from more than 200 causative mutations in the β‐globin gene. In Tunisia, β‐thalassemia represents the most prevalent monogenic hemoglobin disorder wi...

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Veröffentlicht in:J Clin Lab Anal
Hauptverfasser: Sahli, Chaima Abdelhafidh, Ben Salem, Ikbel, Jouini, Latifa, Laouini, Naouel, Dabboubi, Rym, Hadj Fredj, Sondes, Siala, Hajer, Othmeni, Rym, Dakhlaoui, Boutheina, Fattoum, Slaheddine, Bibi, Amina, Messaoud, Taieb
Format: Artigo
Sprache:Inglês
Veröffentlicht: John Wiley and Sons Inc. 2016
Schlagworte:
Research Articles
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC6807109/
https://ncbi.nlm.nih.gov/pubmed/27086580
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/jcla.21867
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