Glutaric aciduria type I: From clinical, biochemical and molecular diversity to successful therapy-Reference-Cited by-同舟云学术

Glutaric aciduria type I: From clinical, biochemical and molecular diversity to successful therapy

Published:1999-06 Issue:4 Volume:22 Page:381-391
ISSN:0141-8955
Container-title:Journal of Inherited Metabolic Disease
language:en
Short-container-title:J Inherit Metab Dis

Author:

Hoffmann G. F.¹,Zschocke J.¹

Affiliation:

1. ; Department of Neuropaediatrics and Metabolic Diseases; Philipps University; Marburg Germany

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1023/A:1005543904484/fullpdf

Reference30 articles.

1. Gultaric aciduria type 1: enzymatic and neuroradiolagical investigations of two kindreds;Amir;J Pediatr,1989

2. Sensitivity of free and total glutaric and 3-OH-glutaric acid measurements by stable isotopic dilution-assays for the diagnosis of glutaric aciduric type I;Baric;J Inher Metab Dis,1997

3. Diagnosis and management of glutaric aciduria type I;Baric;J Inher Metab Dis,1998

4. Atypical riboflavinresponsive glutaric aciduria, and deficient peroxisomal glutaryl-CoA oxidase activity: a new peroxisomal disorder;Bennett;J Inher Metab Dis,1991

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