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Response to: POLG1 variants can at most cause MNGIE-like but not classic MNGIE phenotypes.
Altuntas, Cansu; Uzunhan, Tugce Aksu; Ertürk, Biray; Petmezci, Mey Talip; Çakar, Nafiye Emel; Noyan, Bilge; Dokucu, Ali Ihsan; Önal, Hasan.
Afiliação
  • Altuntas C; Istinye University Medical Faculty, Pediatric Gastroenterology Department, Istanbul, Turkey.
  • Uzunhan TA; Cemil Tasçioglu City Hospital, Pediatric Neurology Department, Istanbul, Turkey.
  • Ertürk B; Cemil Tasçioglu City Hospital, Medical Genetics Department, Istanbul, Turkey.
  • Petmezci MT; Cemil Tasçioglu City Hospital, Pediatric Intensive Care Department, Istanbul, Turkey.
  • Çakar NE; Cemil Tasçioglu City Hospital, Pediatric Metabolic Diseases Department, Istanbul, Turkey.
  • Noyan B; University of Health Sciences Basaksehir Çam Sakura City Hospital, Pediatric Metabolic Diseases Department, Istanbul, Turkey.
  • Dokucu AI; Cemil Tasçioglu City Hospital, Pediatric Surgery Department, Istanbul, Turkey.
  • Önal H; University of Health Sciences Basaksehir Çam Sakura City Hospital, Pediatric Metabolic Diseases Department, Istanbul, Turkey.
Clin Neurol Neurosurg ; 236: 107893, 2024 Jan.
Article em En | MEDLINE | ID: mdl-37455189
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Pseudo-Obstrução Intestinal / Oftalmoplegia / Encefalomiopatias Mitocondriais / Distrofia Muscular Oculofaríngea Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Pseudo-Obstrução Intestinal / Oftalmoplegia / Encefalomiopatias Mitocondriais / Distrofia Muscular Oculofaríngea Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article