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Article

Rapid single nucleotide polymorphism analysis by primer extension and capillary electrophoresis using polyvinyl pyrrolidone matrix.

Electrophoresis - 1 Jan 2001

Barta C, Ronai Z, Sasvari-Szekely M, Guttman A

Abstract excerpt

Rapid molecular diagnosis of 21-hydroxylase deficiency by detecting the most common mutation in the 21-hydroxylase gene is presented using primer extension and capillary electrophoresis with a polyvinyl pyrrolidone matrix. DNA samples were subjected to polymerase chain reaction (PCR) in order to amplify a 422 bp fragment of the CYP21 gene containing the single nucleotide polymorphism (SNP) site. This product...

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Source

Identifiers

PMID: 11296934
DOI: 10.1002/1522-2683(200102)22:4<779::AID-ELPS779>3.0.CO;2-4

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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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