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Encephalopathy, kidney failure and retinopathy. CoQ10 deficiency due to COQ8B mutation.
Adán Lanceta, Victor; Romero Salas, Yolanda; Justa Roldán, María Luisa; García Jiménez, María Concepción; Ariceta Iraola, Gema.
Affiliation
  • Adán Lanceta V; Servicio de Pediatría, Hospital Obispo Polanco, Teruel, Spain. Electronic address: victoradanlanceta@gmail.com.
  • Romero Salas Y; Unidad de Nefrología Pediátrica, Hospital Infantil Universitario Miguel Servet, Zaragoza, Spain.
  • Justa Roldán ML; Unidad de Nefrología Pediátrica, Hospital Infantil Universitario Miguel Servet, Zaragoza, Spain.
  • García Jiménez MC; Unidad de Metabolopatías, Hospital Universitario Miguel Servet, Zaragoza, Spain.
  • Ariceta Iraola G; Servicio de Nefrología Pediátrica, Hospital Vall d'Hebron, Barcelona, Spain.
An Pediatr (Engl Ed) ; 94(6): 415-417, 2021 06.
Article in En | MEDLINE | ID: mdl-34090639
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Retinal Diseases / Brain Diseases / Renal Insufficiency Limits: Humans Language: En Journal: An Pediatr (Engl Ed) Year: 2021 Document type: Article Country of publication: España
Fulltext
Add to My VHL
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Retinal Diseases / Brain Diseases / Renal Insufficiency Limits: Humans Language: En Journal: An Pediatr (Engl Ed) Year: 2021 Document type: Article Country of publication: España