Mechanisms of SSBP1 variants in mitochondrial disease: Molecular dynamics simulations reveal stable tetramers with altered DNA binding surfaces
Author:
Funder
National Institutes of Health
National Institute of Environmental Health Sciences
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference31 articles.
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3. Heterozygous SSBP1 start loss mutation co-segregates with hearing loss and the m.1555A&G mtDNA variant in a large multigenerational family;Kullar;Brain,2018
4. SSBP1 mutations in dominant optic atrophy with variable retinal degeneration;Jurkute;Ann. Neurol.,2019
5. Mitochondrial single-stranded DNA binding protein novel de novo SSBP1 mutation in a child with single large-scale mtDNA deletion (SLSMD) clinically manifesting as Pearson, Kearns-Sayre, and Leigh syndromes;Gustafson;PLoS One,2019
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