Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Esperanza Palacios Valverde"'
Autor:
Sinziana Stanescu, Amaya Belanger-Quintana, Carlos Alcalde Martin, Celia Pérez-Cerdá Silvestre, Begoña Merinero Cortés, Belen Gonzalez Pérez, Carmen Fernández García-Abril, Francisco Arrieta Blanco, Esperanza Palacios Valverde, Mercedes Martínez-Pardo Casanova
Publikováno v:
Case Reports in Pediatrics, Vol 2020 (2020)
Background. Multiple acyl-CoA dehydrogenase deficiency is an autosomal recessive disorder of the amino acid metabolism and fatty acid oxidation due to the deficiency of the electron transfer protein or electron transfer protein ubiquinone oxidoreduct
Externí odkaz:
https://doaj.org/article/c53ac6959a3041ea8f88045bc8ffe8da
Autor:
Belen Gonzalez Pérez, Mercedes Martínez-Pardo Casanova, Carmen Fernández García-Abril, Celia Pérez-Cerdá Silvestre, Sinziana Stanescu, Esperanza Palacios Valverde, Amaya Belanger-Quintana, Francisco Arrieta Blanco, Begoña Merinero Cortés, Carlos Alcalde Martin
Publikováno v:
Case Reports in Pediatrics
Case Reports in Pediatrics, Vol 2020 (2020)
Case Reports in Pediatrics, Vol 2020 (2020)
Background. Multiple acyl-CoA dehydrogenase deficiency is an autosomal recessive disorder of the amino acid metabolism and fatty acid oxidation due to the deficiency of the electron transfer protein or electron transfer protein ubiquinone oxidoreduct
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bb831cb6be66bb5fa8e9acaad53a524b
http://europepmc.org/articles/PMC7378605
http://europepmc.org/articles/PMC7378605