823 3-METHYLGLUTACONYL-CoA HYDRATASE DEFICIENCY: TWO DIFFERENT CLINICAL AND ENZYMATIC PHENOTYPES IN 3-METHYLGLUTACONIC ACIDURIA-Reference-Cited by-同舟云学术

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823 3-METHYLGLUTACONYL-CoA HYDRATASE DEFICIENCY: TWO DIFFERENT CLINICAL AND ENZYMATIC PHENOTYPES IN 3-METHYLGLUTACONIC ACIDURIA

Published:1985-04 Issue:4 Volume:19 Page:248A-248A
ISSN:0031-3998
Container-title:Pediatric Research
language:
Short-container-title:Pediatr Res

Author:

Gibson K M,Sweetsman L,Nyhan W L,Narisawa K,Roth K,Lehnert W,Robinson B,Duran M,Wadman S K

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology, and Child Health

Cited by 7 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Acute Encephalopathic Presentation of 3-Methylglutaconic Aciduria Type I With a Novel Mutation in AUH Gene;Cureus;2020-12-07

2. Early infantile presentation of 3-methylglutaconic aciduria type 1 with a novel mutation in AUH gene: A case report and literature review;Brain and Development;2017-09

3. 3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency: review of 18 reported patients;European Journal of Pediatrics;1988-12

4. 3-Methylglutaconic aciduria: a phenotype in which activity of 3-methylglutaconyl-coenzyme A hydratase is normal;European Journal of Pediatrics;1988-10

5. 3-Methylglutaconic aciduria: Familial neonatal form with fatal onset;Journal of Inherited Metabolic Disease;1987-06

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