المؤلفون: Wichit Suthammarak, Chalermchai Mitrpant, Sukanya Ruchadaariyachat, Supannee Kaewsutthi, Harald Grove, Patcharee Lertrit, Bhoom Suktitipat, Wanicha Chuenkongkaew, Jarichad Toosaranont, Khin Kay Zin Tun

مصطلحات موضوعية: Genetics, Whole genome sequencing, congenital, hereditary, and neonatal diseases and abnormalities, genetic structures, Leber's hereditary optic neuropathy, nutritional and metabolic diseases, Prostanoid, Biology, medicine.disease, eye diseases, Transcriptome, chemistry.chemical_compound, chemistry, Mutation (genetic algorithm), medicine, Receptor

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::341a7c20512ca653c8ecf8fcbf1c8eef
https://doi.org/10.21203/rs.3.rs-604500/v1