Duchenne muscular dystrophy, glycerol kinase deficiency, and adrenal insufficiency associated with Xp21 interstitial deletion
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology and Child Health
Reference14 articles.
1. Localization of DNA sequences in region Xp21 of the human X chromosome: search for molecular markers close to the Duchenne muscular dystrophy locus;De Martinville;Am J Hum Genet,1985
2. Familial hyperglycerolemia;Rose;J Clin Invest,1978
3. Concordance of X-linked glycerol kinase deficiency with X-linked congenital adrenal hypoplasia;Bartley;Lancet,1982
4. Human glycerol kinase deficiency: an inborn error of compartmental metabolism;McCabe;Biochem Med,1983
5. A juvenile form of glycerol kinase deficiency with episodic vomiting, acidemia, and stupor;Ginns;J Pediatr,1984
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