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Prospects of carrie...
Prospects of carrier screening of aspartylglucosaminuria in Finland
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Hietala, M (author)
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Grön, K (author)
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Syvänen, Ann-Christine (author)
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Peltonen, L (author)
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Aula, P (author)
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- 1993
- 1993
- English.
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In: European Journal of Human Genetics. - 1018-4813 .- 1476-5438. ; 1:4, s. 296-300
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https://urn.kb.se/re...
Abstract
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- The frequency of carriers of the AGUFin mutation, the predominant mutation causing aspartylglucosaminuria in Finland, was determined in a population sample comprising 553 newborns from a delivery hospital in southern Finland, and 607 from a hospital in northern Finland. The AGUFin point mutation was identified from cord blood samples using the PCR-based, solid-phase minisequencing method. Nineteen carriers of the AGUFin mutation were detected, 8 (1:69) in the sample from the southern and 11 (1:55) from the northern population, respectively. The solid-phase minisequencing method proved to be rapid and convenient for the detection of the AGUFin mutation, and can readily be applied in large-scale carrier screening at the population level.
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- ref (subject category)
- art (subject category)
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