Author:
Pastore Anna,Petrillo Sara,Tozzi Giulia,Carrozzo Rosalba,Martinelli Diego,Dionisi-Vici Carlo,Di Giovamberardino Gianna,Ceravolo Ferdinando,Klein Matthew B.,Miller Guy,Enns Gregory M.,Bertini Enrico,Piemonte Fiorella
Subject
Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism
Reference34 articles.
1. Mitochondrial energetics and therapeutics;Wallace;Annu. Rev. Pathol.,2010
2. Subacute necrotizing encephalomyelopathy in an infant;Leigh;J. Neurol. Neurosurg. Psychiatry,1951
3. The mutation at NT-8993 of mitochondrial-DNA is a common-cause of Leigh's syndrome;Santorelli;Ann. Neurol.,1993
4. Syndrome Leigh caused by mutations in the SURF1 gene: clinical and molecular-genetic characteristics;Tsygankova;Zh. Nevrol. Psikhiatr. Im. S. S. Korsakova,2010
5. High prevalence of SURF1 c.845_846delCT mutation in Polish Leigh patients;Piekutowska-Abramczuk;Eur. J. Paediatr. Neurol.,2009
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