Multiplex Minisequencing Screen for Common Southeast Asian and Indian β-Thalassemia Mutations
Multiplex Minisequencing Screen for Common Southeast Asian and Indian β-Thalassemia Mutations
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Washington, DC: American Association for Clinical Chemistry
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English
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Washington, DC: American Association for Clinical Chemistry
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Background: β-Thalassemia is endemic to many regions in Southeast Asia and India, and <20 β-globin gene mutations account for ≥90% of β-thalassemia alleles in these places. We describe a multiplex minisequencing assay to detect these common mutations.
Methods: Gap-PCR was used to simultaneously amplify the β-globin gene from genomic DNA and to d...
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Full title
Multiplex Minisequencing Screen for Common Southeast Asian and Indian β-Thalassemia Mutations
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TN_cdi_proquest_miscellaneous_72982496
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_72982496
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ISSN
0009-9147
E-ISSN
1530-8561
DOI
10.1373/49.2.209
