A New Mitochondrial DNA Mutation in ND3 Gene Causing Severe Leigh Syndrome with Early Lethality-Reference-Cited by-同舟云学术

A New Mitochondrial DNA Mutation in ND3 Gene Causing Severe Leigh Syndrome with Early Lethality

Published:2004-05 Issue:5 Volume:55 Page:842-846
ISSN:0031-3998
Container-title:Pediatric Research
language:
Short-container-title:Pediatr Res

Author:

Crimi Marco,Papadimitriou Alexandros,Galbiati Sara,Palamidou Phani,Fortunato Francesco,Bordoni Andreina,Papandreou Urania,Papadimitriou Dimitra,Hadjigeorgiou George M,Drogari Eurydiki,Bresolin Nereo,Comi Giacomo Pietro

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology, and Child Health

Reference20 articles.

1. SUBACUTE NECROTIZING ENCEPHALOMYELOPATHY IN AN INFANT

2. Mitochondrial Respiratory-Chain Diseases

3. Isolated complex I deficiency in children: Clinical, biochemical and genetic aspects

4. Nuclear genetic defects of oxidative phosphorylation

5. A collection of 33 novel human mtDNA homoplasmic variants

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