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Kearns-Sayre syndrome case. Novel 5,9 kb mtDNA deletion.
Grigalioniene, Kristina; Burnyte, Birute; Balkeliene, Danute; Ambrozaityte, Laima; Utkus, Algirdas.
Affiliation
  • Grigalioniene K; Department of Human and Medical Genetics, Institute of Biomedical Sciences, Faculty of Medicine, Vilnius University, Vilnius, Lithuania.
  • Burnyte B; Department of Human and Medical Genetics, Institute of Biomedical Sciences, Faculty of Medicine, Vilnius University, Vilnius, Lithuania.
  • Balkeliene D; Department of Human and Medical Genetics, Institute of Biomedical Sciences, Faculty of Medicine, Vilnius University, Vilnius, Lithuania.
  • Ambrozaityte L; Department of Human and Medical Genetics, Institute of Biomedical Sciences, Faculty of Medicine, Vilnius University, Vilnius, Lithuania.
  • Utkus A; Department of Human and Medical Genetics, Institute of Biomedical Sciences, Faculty of Medicine, Vilnius University, Vilnius, Lithuania.
Mol Genet Genomic Med ; 11(1): e2059, 2023 01.
Article in En | MEDLINE | ID: mdl-36181358
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Kearns-Sayre Syndrome / Ophthalmoplegia, Chronic Progressive External Limits: Adult / Humans / Male Language: En Journal: Mol Genet Genomic Med Year: 2023 Document type: Article Affiliation country: Country of publication:
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Kearns-Sayre Syndrome / Ophthalmoplegia, Chronic Progressive External Limits: Adult / Humans / Male Language: En Journal: Mol Genet Genomic Med Year: 2023 Document type: Article Affiliation country: Country of publication: