Long-term outcome of Leigh syndrome caused by the NARP-T8993C mtDNA mutation
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Reference31 articles.
1. A family with Leigh syndrome caused by the rarer T8993C mutation
2. Mitochondrial Uncoupling Protein-4 Regulates Calcium Homeostasis and Sensitivity to Store Depletion-induced Apoptosis in Neural Cells
3. A second missense mutation in the mitochondrial ATPase 6 gene in Leigh's syndrome
4. Mitochondrial DNA 8993 (NARP) mutation presenting with a heterogeneous phenotype including 'cerebral palsy'.
5. Phenotypic Differences Between T → C and T → G Mutations at nt 8993 of Mitochondrial DNA in Leigh Syndrome
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