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Article

Detection of four beta-thalassemia point mutations in Iranians using a PCR-ELISA genotyping system.

Molecular and cellular probes - 1 Apr 2008

Gill Pooria, Forouzandeh Mehdi, Eshraghi Naser, Ghalami Mostafa, Safa Majid, Noori-Daloii Mohammad-Reza

Abstract excerpt

Development of molecular techniques with analytical capability of mutation detection can realize the medical diagnosis of diseases and improve people's health. beta-Thalassemia is one of the most prevalent genetic disorders in Iran and using a simple and rapid test in laboratories for the mass screening and prenatal diagnosis is essential. Here, we described a simple method for rapid detection of four common...

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PMID: 18036776
DOI: 10.1016/j.mcp.2007.10.001

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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