A neonatal case of 3-hydroxy-3-methylglutaric-coenzyme A lyase deficiency-Reference-Cited by-同舟云学术

A neonatal case of 3-hydroxy-3-methylglutaric-coenzyme A lyase deficiency

Published:2013 Issue:1 Volume:39 Page:33
ISSN:1824-7288
Container-title:Italian Journal of Pediatrics
language:en
Short-container-title:Ital J Pediatr

Author:

Santarelli Francesca,Cassanello Michela,Enea Ausilia,Poma Francesca,D'Onofrio Valentina,Guala Giovanna,Garrone Giangiacomo,Puccinelli Paola,Caruso Ubaldo,Porta Francesco,Spada Marco

Publisher

Springer Science and Business Media LLC

Subject

General Medicine

Reference4 articles.

1. 3-Hydroxy-3-methylglutaryl-coenzyme A lyase deficiency: Initial presentation in a young adult

2. Molecular genetics of HMG-CoA lyase deficiency

3. A Case of Dilated Cardiomyopathy Associated with 3-Hydroxy-3-Methylglutaryl-Coenzyme A (HMG CoA) Lyase Deficiency

4. Differential HMG-CoA lyase expression in human tissues provides clues about 3-hydroxy-3-methylglutaric aciduria

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