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pro vyhledávání: '"Zaure Mussakhanova"'
Autor:
Zaure Mussakhanova, Ardak Orazbay, Tamara Ermakhanova, Oral Onlassynova, Malika Akhmerova, Aluash Satybaldina, Aikerim Slamova, Rimma Bazarbekova, Ayaulym Alpan
Publikováno v:
Journal "Medicine". :26-32
21-hydroxylase deficiency is the cause of one of the most common hereditary diseases - congenital adrenal hyperplasia (CAH). The level of residual activity of 21-hydroxylase determines the clinical form and severity of the course of the disease. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::462d970c7f3bb43fcb9fc95e051cc690
https://doi.org/10.31082/1728-452x-2020-213-214-3-4-26-32
https://doi.org/10.31082/1728-452x-2020-213-214-3-4-26-32
