Duchenne muscular dystrophy, glycerol kinase deficiency, and adrenal insufficiency associated with Xp21 interstitial deletion-Reference-Cited by-同舟云学术

Duchenne muscular dystrophy, glycerol kinase deficiency, and adrenal insufficiency associated with Xp21 interstitial deletion

Published:1986-02 Issue:2 Volume:108 Page:189-192
ISSN:0022-3476
Container-title:The Journal of Pediatrics
language:en
Short-container-title:The Journal of Pediatrics

Author:

Bartley James A.,Patil Shivanand,Davenport Sandra,Goldstein David,Pickens James

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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