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Should Patients with Kearns-Sayre Syndrome and Corneal Endothelial Failure Be Genotyped for a TCF4 Trinucleotide Repeat, Commonly Associated with Fuchs Endothelial Corneal Dystrophy?
Genes (Basel). 2021 Nov 29;12(12):1918. doi: 10.3390/genes12121918.
Genes (Basel). 2021.
PMID: 34946867
Free PMC article.
The Phenotypic Spectrum of 47 Czech Patients with Single, Large-Scale Mitochondrial DNA Deletions.
Anteneová N, Kelifová S, Kolářová H, Vondráčková A, Tóthová I, Lišková P, Magner M, Zámečník J, Hansíková H, Zeman J, Tesařová M, Honzík T.
Anteneová N, et al.
Brain Sci. 2020 Oct 22;10(11):766. doi: 10.3390/brainsci10110766.
Brain Sci. 2020.
PMID: 33105723
Free PMC article.
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