Complex III deficiency in a Portuguese family: expanding the clinical phenotype

http://hdl.handle.net/10400.18/2166

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Authors

Nogueira, Célia

Meschini, M. Clara

Carrozzo, Rosalba

Sá, Maria José

Santorelli, Filippo

Vilarinho, Laura

Keywords

CIII Doenças Genéticas

URI

http://hdl.handle.net/10400.18/2166

Collections

DGH - Posters/abstracts em congressos internacionais