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Clinical, genetic, and structural basis of apparent mineralocorticoid excess due to 11β-hydroxysteroid dehydrogenase type 2 deficiency.
Proc Natl Acad Sci U S A. 2017 Dec 26;114(52):E11248-E11256. doi: 10.1073/pnas.1716621115. Epub 2017 Dec 11.
Proc Natl Acad Sci U S A. 2017.
PMID: 29229831
Free PMC article.
Clinical characteristics and phenotype-genotype review of 25 Omani children with congenital hyperinsulinism in infancy. A one-decade single-center experience.
Al-Badi MK, Al-Azkawi HS, Al-Yahyaei MS, Mula-Abed WA, Al-Senani AM.
Al-Badi MK, et al. Among authors: al azkawi hs.
Saudi Med J. 2019 Jul;40(7):669-674. doi: 10.15537/smj.2019.7.24291.
Saudi Med J. 2019.
PMID: 31287126
Free PMC article.
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