Author:
AlMenabawy Nihal,Hassaan Hebatallah M,Ramadan Manal,Ehsan Abdel Meguid Iman,Ahmed El Gindy Hala,Beetz Christian,Selim Laila
Subject
Cell Biology,Molecular Biology,Molecular Medicine
Reference35 articles.
1. Clinical and molecular characteristics of mitochondrial DNA depletion syndrome associated with neonatal cholestasis and liver failure;Al-Hussaini;J. Pediatr.,2014
2. Almannai, M., Dai, H., El- Hattab, A. W. & Wong, L.-J. C. FBXL4 -Related Encephalomyopathic Mitochondrial DNA Depletion Syndrome. in GeneReviews (2017).
3. FBXL4-related mitochondrial DNA depletion syndrome 13 (MTDPS13): a case report with a comprehensive mutation review;Ballout;Front. Genet.,2019
4. Adult cases of mitochondrial DNA depletion due to TK2 defect: an expanding spectrum;Behin;Neurology,2012
5. A homozygous mutation in INVS causing juvenile nephronophthisis with abnormal reactivity of the Wnt/beta-catenin pathway;Bellavia;Nephrol. Dial. Transplant.,2010
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