A Novel Mutation in an MNGIE Patient Presenting with More Prominent Neurological Symptoms than GI Symptoms
Author:
Publisher
Medknow
Subject
Neurology (clinical),Neurology
Reference6 articles.
1. Next generation sequencing in family with MNGIE syndrome associated to optic atrophy: Novel homozygous POLG mutation in the C-terminal sub-domain leading to mtDNA depletion;Felhi;Clin Chim Acta,2019
2. Mitochondrial neurogastrointestinal encephalopathy: A clinicopathological mimic of Crohn's disease;Patel;BMC Gastroenterol,2019
3. Mitochondrial neurogastrointestinal encephalomyopathy presenting as Anorexia Nervosa;Demaria;J Adolesc Health,2016
4. Mitochondrial neurogastrointestinal encephalopathy (MNGIE) in a South Indian family with two affected siblings;Santoshkumar;Neurol India,1997
5. Mitochondrial neurogastrointestinal encephalomyopathy imitating Crohn's disease: A rare cause of malnutrition;Kucerova;J Gastrointestin Liver Dis,2018
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