Molybdenum cofactor deficiency-Reference-Cited by-同舟云学术

Molybdenum cofactor deficiency

Published:1993-10 Issue:4 Volume:123 Page:595-598
ISSN:0022-3476
Container-title:The Journal of Pediatrics
language:en
Short-container-title:The Journal of Pediatrics

Author:

Arnold Georgianne L.,Greene Carol L.,Patrick Stout J.,Goodman Stephen I.

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology, and Child Health

Reference17 articles.

1. Combined deficiency of xanthine oxidase and sulphite oxidase: a defect of molybdenum metabolism or transport?;Duran;J Inherit Metab Dis,1978

2. Johnson JL, Wadman SK. Molybdenum cofactor deficiency.In: Scriver CR, Beaudet AL, Sly WS, Valle D, eds. The metabolic basis of inherited disease. 7th ed. New York: McGraw-Hill (in press).

3. 2-Mercaptoethane-sulfonate-cysteine disulfide excretion following the administration of 2-mercaptoethanesulfonate: a pitfall in the diagnosis of sulfite oxidase deficiency;Duran;Clin Chim Acta,1981

4. Sulfite oxidase deficiency and the detection of urinary sulfite;Wadman;Eur J Pediatr,1983

5. Molybdenum cofactor deficiency: an easily missed inborn error of metabolism;Aukett;Dev Med Child Neurol,1988

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