Author:
Telerman-Toppet N.,Biarent D.,Bouton J. -M.,de Meirleir L.,Elmer C.,Noel S.,Vamos E.,DiMauro S.
Subject
Genetics(clinical),Genetics
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2. Moraes CT, Shanske S, Tritschler HJ et al (1991) mtDNA depletion with variable tissue expression: a novel genetic abnormality in mitochondrial diseases.Am J Hum Genet 48: 492–501.
3. Tritschler HJ, Bonilla E, Lombes A et al (1991) Differential diagnosis of fatal and benign cytochromec oxidase-deficient myopathies of infancy: an immunohistochemical approach.Neurology 41: 300–305.
4. Zeviani M, Servidei S, Gellera C, Bertini E, DiMauro S, DiDonato S (1989) An autosomal dominant disorder with multiple deletions of mitochondrial DNA starting at the D-loop region.Nature 339: 309–311.
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