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Sistani population: a different spectrum of β-thalassemia mutations from other ethnic groups of Iran.

Hemoglobin - 1 Jan 2013

Miri-Moghaddam Ebrahim, Zadeh-Vakili Azita, Nikravesh Abbas, Sistani Shohreh Sanei, Naroie-Nejad Mehrnaz

Abstract excerpt

This study aimed to characterize the molecular spectrum of β-thalassemia (β-thal) mutations and evaluate the services available for prenatal diagnosis (PND) among the Sistani population of Iran. Mutations were analyzed with amplification refractory mutation system (ARMS), gap-polymerase chain reaction (gap-PCR), multiplex ligation-dependent probe amplification (MLPA) analysis and direct sequencing. Fetal...

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PMID: 23437895
DOI: 10.3109/03630269.2013.769886

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

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