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pro vyhledávání: '"Xochitl Felix-Lopez"'
Autor:
Ma. Luisa Ordonez-Sanchez, Xochitl Felix-Lopez, Ma. Teresa Tusié-Luna, Alejandro Zentella-Dehesa, Salvador Ramírez-Jiménez, José Luis Ventura-Gallegos, Laura Riba
Publikováno v:
Journal of pediatric endocrinologymetabolism : JPEM. 16(7)
Steroid 21-hydroxylase deficiency is the major cause of congenital adrenal hyperplasia, an autosomic recessive disorder that affects the synthesis of aldosterone and cortisol. The disease presents a wide spectrum of clinical phenotypes as a result of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d007492d0ff88e6fdd86bd958cccd28
https://pubmed.ncbi.nlm.nih.gov/14513879
https://pubmed.ncbi.nlm.nih.gov/14513879
