Galt enzyme deficiency identification in newborns in Azerbaijan

Автор: Hajiyeva Nilufar

Журнал: Бюллетень науки и практики @bulletennauki

Статья в выпуске: 9 т.8, 2022 года.

Бесплатный доступ

For the first time in Baku, Azerbaijan Republic in maternity houses by means of immunoenzyme analysis the genetic screening for galactosemia inherited metabolism disorder was carried out, and 3 newborns with GALT gene deficiency for were identified.

Duarte galactosemia, metabolism disorder, enzyme of galactose-1-phosphaturidyltransferase, polymerase chain reaction, mutation

Короткий адрес: https://sciup.org/14125319

IDR: 14125319 | DOI: 10.33619/2414-2948/82/32

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