A case of mitochondrial DNA depletion syndrome type 11 - expanding the genotype and phenotype
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Published in: | Neuromuscular disorders : NMD Vol. 33; no. 8; pp. 692 - 696 |
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Main Authors: | , , , , , , , , , |
Format: | Report |
Language: | English |
Published: |
01-08-2023
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Author | Graca, Carla Renata Estephan, Eduardo de Paula Coelho, Érica Nogueira Nóbrega, Paulo Ribeiro de Lima Rodrigues, Ketteny Montouro, Laura Alonso Matheus Kok, Fernando Morita, Maria da Penha Ananias da Silva Rocha, Emanuelle Bianchi Kouyoumdjian, João Aris |
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Author_xml | – sequence: 1 givenname: Emanuelle Bianchi surname: da Silva Rocha fullname: da Silva Rocha, Emanuelle Bianchi – sequence: 2 givenname: Ketteny surname: de Lima Rodrigues fullname: de Lima Rodrigues, Ketteny – sequence: 3 givenname: Laura Alonso Matheus surname: Montouro fullname: Montouro, Laura Alonso Matheus – sequence: 4 givenname: Érica Nogueira surname: Coelho fullname: Coelho, Érica Nogueira – sequence: 5 givenname: João Aris surname: Kouyoumdjian fullname: Kouyoumdjian, João Aris – sequence: 6 givenname: Fernando surname: Kok fullname: Kok, Fernando – sequence: 7 givenname: Paulo Ribeiro surname: Nóbrega fullname: Nóbrega, Paulo Ribeiro – sequence: 8 givenname: Carla Renata surname: Graca fullname: Graca, Carla Renata – sequence: 9 givenname: Maria da Penha Ananias surname: Morita fullname: Morita, Maria da Penha Ananias – sequence: 10 givenname: Eduardo de Paula surname: Estephan fullname: Estephan, Eduardo de Paula |
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Title | A case of mitochondrial DNA depletion syndrome type 11 - expanding the genotype and phenotype |
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