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pro vyhledávání: '"Asanak Sudeshini Hewage"'
Publikováno v:
The Ceylon medical journal. 65(4)
Introduction: Steroid hydroxylase deficiency due to CYP21A2 gene mutation is the most common cause of Congenital Adrenal Hyperplasia (CAH). Mutation spectrum in Sri Lankan CAH patients has not been investigated adequately. Objectives: This study atte
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::89ddb72bac24a5880ad8dfb4a1240f6d
https://pubmed.ncbi.nlm.nih.gov/34821488
https://pubmed.ncbi.nlm.nih.gov/34821488
