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World Journal of Clinical Cases|September 2, 2022
Clinical expression and mitochondrial deoxyribonucleic acid study in twins with 14484 Leber's hereditary optic neuropathy: A case reportWanicha Leetiratanai Chuenkongkaew, Buakhwan Chinkulkitnivat, Patcharee Lertrit, et al.
Investigative Ophthalmology & Visual Science|March 15, 2011
Mitochondrial haplogroup background may influence Southeast Asian G11778A Leber hereditary optic neuropathySupannee Kaewsutthi, Nopasak Phasukkijwatana, Yutthana Joyjinda, et al.
Frontiers in Pediatrics|June 10, 2022
Association of Mitochondrial DNA Polymorphisms With Pediatric-Onset Cyclic Vomiting SyndromeKirana Veenin, Duangrurdee Wattanasirichaigoon, Bhoom Suktitipat, et al.
Experimental Eye Research|August 27, 2013
Identification of the variants in PARL, the nuclear modifier gene, responsible for the expression of LHON patients in ThailandRochmy Istikharah, Aung Win Tun, Supannee Kaewsutthi, et al.
Investigative Ophthalmology & Visual Science|April 29, 2017
Whole Exome Sequencing in Eight Thai Patients With Leber Congenital Amaurosis Reveals Mutations in the CTNNA1 and CYP4V2 GenesWorapoj Jinda, Todd D Taylor, Yutaka Suzuki, et al.
Forensic Science International. Genetics|April 22, 2014
Development of a SNP set for human identification: A set with high powers of discrimination which yields high genetic information from naturally degraded DNA samples in the Thai populationHathaichanoke Boonyarit, Surakameth Mahasirimongkol, Nuttama Chavalvechakul, et al.
Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society|January 6, 2007
Mitochondrial DNA haplogroup distribution in pedigrees of Southeast Asian G11778A Leber hereditary optic neuropathyPattamon Tharaphan, Wanicha L Chuenkongkaew, Komon Luangtrakool, et al.
Investigative Ophthalmology & Visual Science|March 13, 2014
Whole exome sequencing in Thai patients with retinitis pigmentosa reveals novel mutations in six genesWorapoj Jinda, Todd D Taylor, Yutaka Suzuki, et al.
Molecular Vision|April 29, 2016
A novel start codon mutation of the MERTK gene in a patient with retinitis pigmentosaWorapoj Jinda, Naravat Poungvarin, Todd D Taylor, et al.
Plos One|September 13, 2014
Profiling the mitochondrial proteome of Leber's Hereditary Optic Neuropathy (LHON) in Thailand: down-regulation of bioenergetics and mitochondrial protein quality control pathways in fibroblasts with the 11778G>A mutationAung Win Tun, Sakdithep Chaiyarit, Supannee Kaewsutthi, et al.
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