Clinical expression and mitochondrial deoxyribonucleic acid study in twins with 14484 Leber’s hereditary optic neuropathy: A case report

por Chuenkongkaew, Wanicha Leetiratanai, Chinkulkitnivat, Buakhwan, Lertrit, Patcharee, Chirapapaisan, Niphon, Kaewsutthi, Supannee, Suktitipat, Bhoom, Mitrpant, Chalermchai
Publicado 2022

Association of Mitochondrial DNA Polymorphisms With Pediatric-Onset Cyclic Vomiting Syndrome

por Veenin, Kirana, Wattanasirichaigoon, Duangrurdee, Suktitipat, Bhoom, Noojarern, Saisuda, Lertrit, Patcharee, Tim-Aroon, Thipwimol, Kaewsutthi, Supannee, Treepongkaruna, Suporn
Publicado 2022

A novel start codon mutation of the MERTK gene in a patient with retinitis pigmentosa

por Jinda, Worapoj, Poungvarin, Naravat, Taylor, Todd D., Suzuki, Yutaka, Thongnoppakhun, Wanna, Limwongse, Chanin, Lertrit, Patcharee, Suriyaphol, Prapat, Atchaneeyasakul, La-ongsri
Publicado 2016

Profiling the Mitochondrial Proteome of Leber’s Hereditary Optic Neuropathy (LHON) in Thailand: Down-Regulation of Bioenergetics and Mitochondrial Protein Quality Control Pathways...

por Tun, Aung Win, Chaiyarit, Sakdithep, Kaewsutthi, Supannee, Katanyoo, Wanphen, Chuenkongkaew, Wanicha, Kuwano, Masayoshi, Tomonaga, Takeshi, Peerapittayamongkol, Chayanon, Thongboonkerd, Visith, Lertrit, Patcharee
Publicado 2014