Response to: POLG1 variants can at most cause MNGIE-like but not classic MNGIE phenotypes.

Autor: Altuntaş C; İstinye University Medical Faculty, Pediatric Gastroenterology Department, Istanbul, Turkey., Uzunhan TA; Cemil Taşçıoğlu City Hospital, Pediatric Neurology Department, Istanbul, Turkey., Ertürk B; Cemil Taşçıoğlu City Hospital, Medical Genetics Department, Istanbul, Turkey., Petmezci MT; Cemil Taşçıoğlu City Hospital, Pediatric Intensive Care Department, Istanbul, Turkey., Çakar NE; Cemil Taşçıoğlu City Hospital, Pediatric Metabolic Diseases Department, Istanbul, Turkey., Noyan B; University of Health Sciences Başakşehir Çam Sakura City Hospital, Pediatric Metabolic Diseases Department, Istanbul, Turkey., Dokucu Aİ; Cemil Taşçıoğlu City Hospital, Pediatric Surgery Department, Istanbul, Turkey., Önal H; University of Health Sciences Başakşehir Çam Sakura City Hospital, Pediatric Metabolic Diseases Department, Istanbul, Turkey.
Jazyk: angličtina
Zdroj: Clinical neurology and neurosurgery [Clin Neurol Neurosurg] 2024 Jan; Vol. 236, pp. 107893. Date of Electronic Publication: 2023 Jul 13.
DOI: 10.1016/j.clineuro.2023.107893
Databáze: MEDLINE
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