Open AccessClinical expression and mitochondrial deoxyribonucleic acid study in twins with 14484 Leber’s hereditary optic neuropathy: A case report
Author(s) -
Wanicha Chuenkongkaew,
Buakhwan Chinkulkitnivat,
Patcharee Lertrit,
Niphon Chirapapaisan,
Supannee Kaewsutthi,
Bhoom Suktitipat,
Chalermchai Mitrpant
Publication year - 2022
Publication title -
world journal of clinical cases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.368
H-Index - 10
ISSN - 2307-8960
DOI - 10.12998/wjcc.v10.i20.6944
Subject(s) - heteroplasmy , mitochondrial dna , leber's hereditary optic neuropathy , point mutation , genetics , optic neuropathy , monozygotic twin , non mendelian inheritance , medicine , nuclear dna , mutation , zygosity , epigenetics , mitochondrial disease , microbiology and biotechnology , gene , biology , ophthalmology , optic nerve