Leigh syndrome in an infant resulting from mitochondrial DNA depletion-Reference-Cited by-同舟云学术

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Leigh syndrome in an infant resulting from mitochondrial DNA depletion

Published:2001-01 Issue:1 Volume:24 Page:60-63
ISSN:0887-8994
Container-title:Pediatric Neurology
language:en
Short-container-title:Pediatric Neurology

Author:

Absalon Michael J,Harding Cary O,Fain Daniel R,Li Lei,Mack Kenneth J

Publisher

Elsevier BV

Subject

Clinical Neurology,Developmental Neuroscience,Neurology,Pediatrics, Perinatology, and Child Health

Reference18 articles.

1. Getting to the nucleus of mitochondrial disorders;Dahl;Am J Hum Genet,1998

2. Leigh syndrome;Rahman;Ann Neurol,1996

3. mtDNA depletion with variable tissue expression;Moraes;Am J Hum Genet,1991

4. Clinical heterogeneity associated with mitochondrial DNA depletion in muscle;Campos;Neuromuscul Disord,1998

5. Clinical manifestations of mitochondrial DNA depletion;Vu;Neurology,1998

Cited by 21 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. Developmental anatomy of the thalamus, perinatal lesions, and neurological development;Developmental Medicine & Child Neurology;2024-06-14

2. Muscle Involvement and Restricted Disorders;Volpe's Neurology of the Newborn;2018

3. Degenerative Disorders of the Newborn;Volpe's Neurology of the Newborn;2018

4. Phenotypic and genotypic variability in Alpers syndrome;European Journal of Paediatric Neurology;2012-07

5. Late onset presentation of Leigh syndrome on two cases;Arquivos de Neuro-Psiquiatria;2010-06

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