Clinical expression and mitochondrial deoxyribonucleic acid study in twins with 14484 Leber’s hereditary optic neuropathy: A case report
This study aimed to explore clinical and molecular factors that cause discordance for clinical expression of Leber’s hereditary optic neuropathy (LHON) in a pair of identical twins with the 14484 point mutation. CASE SUMMARY Twin patients with the 14484 point mutation were studied for zygosity by us...
Saved in:
Main Author: | Chuenkongkaew W.L. |
---|---|
Other Authors: | Mahidol University |
Format: | Article |
Published: |
2023
|
Subjects: | |
Online Access: | https://repository.li.mahidol.ac.th/handle/123456789/85714 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Institution: | Mahidol University |
Similar Items
-
Clinical expression and mitochondrial deoxyribonucleic acid study in twins with 14484 Leber’s hereditary optic neuropathy: A case report
by: Wanicha Leetiratanai Chuenkongkaew, et al.
Published: (2022) -
A Thai patient with Leber's hereditary optic neuropathy linked to mitochondrial DNA 14484 mutation
by: Wanicha Chuenkongkaew, et al.
Published: (2018) -
Leber's hereditary optic neuropathy in Thailand
by: Wanicha L. Chuenkongkaew, et al.
Published: (2018) -
Proportion of 11778 mutant mitochondrial DNA and clinical expression in a Thai population with Leber hereditary optic neuropathy
by: Wanicha L. Chuenkongkaew, et al.
Published: (2018) -
The epidemiology and mutation types of Leber’s hereditary optic neuropathy in Thailand
by: Kanchalika Sathianvichitr, et al.
Published: (2022)