Mitochondrial disease in a heteroplasmic MT DNA mutation causing mitochondrial encephalopathy with lactic acidosis and stroke-like episodes (MELAS) and leigh syndrome phenotypes
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
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Online-Ressource
- Sprache
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Englisch
- Erschienen in
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Mitochondrial disease in a heteroplasmic MT DNA mutation causing mitochondrial encephalopathy with lactic acidosis and stroke-like episodes (MELAS) and leigh syndrome phenotypes ; volume:81 ; number:S 01 ; year:2023 ; 01
Konferenz: SBN Conference 2022; 2022-11-09; Expo United Curitiba
Arquivos de neuro-psiquiatria ; 81, Heft S 01 (2023), 01
- Beteiligte Personen und Organisationen
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Dantas, Rafaela Fernandes
Brito, Joemir Jábson da Conceição
Coimbra, Clarice Semiao
Leão, Ana Cristina Azevedo
Barros, Nicholas dos Santos
de Almeida, Roberta Diniz
Cruz, Cristiani Rocha Lima
Bueno, Clarissa
Kok, Fernando
- DOI
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10.1055/s-0043-1774585
- URN
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urn:nbn:de:101:1-2023110211301334263689
- Rechteinformation
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
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14.08.2025, 10:47 MESZ
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Beteiligte
- Dantas, Rafaela Fernandes
- Brito, Joemir Jábson da Conceição
- Coimbra, Clarice Semiao
- Leão, Ana Cristina Azevedo
- Barros, Nicholas dos Santos
- de Almeida, Roberta Diniz
- Cruz, Cristiani Rocha Lima
- Bueno, Clarissa
- Kok, Fernando
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