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Article

Rapid detection of solute carrier family 4, member 1 (SLC4A1) mutations and polymorphisms by high-resolution melting analysis.

Clinical biochemistry - 1 Mar 2010

Nettuwakul Choochai, Sawasdee Nunghathai, Yenchitsomanus Pa-thai

Abstract excerpt

OBJECTIVE: The objective of this study is to develop and evaluate a high-resolution melting (HRM) method for detection of SLC4A1 mutations and polymorphisms. DESIGN AND METHODS: The HRM method was optimized for detection of 18 known SLC4A1 variants. It was then used for analysis of 16 blind DNA samples highly enriched with two common mutations, Southeast Asian ovalocytosis (SAO) and band 3 Bangkok 1 (G701D), to...

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PMID: 20035734
DOI: 10.1016/j.clinbiochem.2009.12.010

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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