Clinical and molecular findings in children with complex I deficiency-Reference-Cited by-同舟云学术

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Clinical and molecular findings in children with complex I deficiency

Published:2004-12 Issue:2-3 Volume:1659 Page:136-147
ISSN:0005-2728
Container-title:Biochimica et Biophysica Acta (BBA) - Bioenergetics
language:en
Short-container-title:Biochimica et Biophysica Acta (BBA) - Bioenergetics

Author:

Bugiani M.,Invernizzi F.,Alberio S.,Briem E.,Lamantea E.,Carrara F.,Moroni I.,Farina L.,Spada M.,Donati M.A.,Uziel G.,Zeviani M.

Publisher

Elsevier BV

Subject

Cell Biology,Biochemistry,Biophysics

Reference43 articles.

1. Leigh syndrome: clinical features and biochemical and DNA abnormalities;Rahman;Ann. Neurol.,1996

2. NADH-coenzyme Q reductase (complex I) deficiency: heterogeneity in phenotype and biochemical findings;Pitkanen;J. Inherit. Metab. Dis.,1996

3. Respiratory chain complex I deficiency: an underdiagnosed energy generation disorder;Kirby;Neurology,1999

4. Isolated complex I deficiency in children: clinical, biochemical and genetic aspects;Loeffen;Hum. Mutat.,2000

5. Analysis of the subunit composition of complex I from bovine heart mitochondria;Carroll;Mol. Cell. Proteomics,2003

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