Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Uttara Adhikari"'
Publikováno v:
Journal of Nepal Medical Association, Vol 58, Iss 221 (2020)
Congenital Adrenal Hyperplasia is a group of autosomal recessive disorders due to deficiencies of enzymes involved in steroidogenesis. The most common form is a 21-hydroxylase deficiency which can be classical or non-classical. The severe form also c
Externí odkaz:
https://doaj.org/article/02b0c711fc1048ab8f33da8d25ff4546
Publikováno v:
JNMA: Journal of the Nepal Medical Association
Journal of Nepal Medical Association, Vol 58, Iss 221 (2020)
Journal of Nepal Medical Association, Vol 58, Iss 221 (2020)
Congenital Adrenal Hyperplasia is a group of autosomal recessive disorders due to deficiencies of enzymes involved in steroidogenesis. The most common form is a 21-hydroxylase deficiency which can be classical or non-classical. The severe form also c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5f0e9ef485538e87079fa8f02f01500a
http://europepmc.org/articles/PMC7580480
http://europepmc.org/articles/PMC7580480