Author:
Saudubray J.M.,Nassogne M.C.,de Lonlay P.,Touati G.
Subject
Pediatrics, Perinatology, and Child Health
Reference11 articles.
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4. Mutations in the NSDHL gene, encoding a 3β-hydroxysteroid dehydrogenase, cause CHILD syndrome;Konig;Am J Hum Genet,2000
5. Inborn errors of cholesterol biosynthesis;Kelley;Adv Pediatr,2000
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