Molecular analysis of Taiwanese patients with 3-Hydroxy-3-methylglutaryl CoA lyase deficiency-Reference-Cited by-同舟云学术

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Molecular analysis of Taiwanese patients with 3-Hydroxy-3-methylglutaryl CoA lyase deficiency

Published:2009-03 Issue:1-2 Volume:401 Page:33-36
ISSN:0009-8981
Container-title:Clinica Chimica Acta
language:en
Short-container-title:Clinica Chimica Acta

Author:

Lin Wei-De,Wang Chung-Hsing,Lai Chien-Chen,Tsai Yushin,Wu Jer-Yuarn,Chen Chih-Ping,Tsai Fuu-Jen

Publisher

Elsevier BV

Subject

Biochemistry (medical),Clinical Biochemistry,Biochemistry,General Medicine

Reference19 articles.

1. Inborn errors of ketone body metabolism;Mitchell,2001

2. The contribution of protein catabolism to metabolic decompensation in 3-hydroxy-3-methylglutaric aciduria;Thompson;Eur J Pediatr,1990

3. 3-Hydroxy-3-methylglutaryl-coenzyme a lyase deficiency: a review;Wysocki;J Inherit Metab Dis,1986

4. 3-Hydroxy-3- methylglutaryl CoA lyase (HL): mouse and human HL gene (HMGCL) cloning and detection of large gene deletions in two unrelated HL-deficient patients;Wang;Genomics,1996

5. 3-Hydroxy-3-methylglutaryl coenzyme A lyase (HL): cloning of human and chicken liver HL cDNAs and characterization of a mutation causing human HL deficiency;Mitchell;J Biol Chem,1993

Cited by 2 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. Inborn Errors of Ketogenesis: Novel Variants, Clinical Presentation, and Follow-Up in a Series of Four Patients;Journal of Pediatric Genetics;2022-07-12

2. 3-Hydroxy-3-methylglutaric aciduria with bilateral basal ganglia lesion: A case report;Experimental and Therapeutic Medicine;2016-04-11

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