Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Netchanok Leela-Adisorn"'
Autor:
Suphalak Chokvithaya, Natarin Caengprasath, Aayalida Buasong, Supavadee Jantasuwan, Kanokwan Santawong, Netchanok Leela-adisorn, Siraprapa Tongkobpetch, Chupong Ittiwut, Vitchayaporn Emarach Saengow, Wuttichart Kamolvisit, Ponghatai Boonsimma, Saknan Bongsebandhu-phubhakdi, Vorasuk Shotelersuk
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-11 (2023)
Abstract Mutations in KCNQ2 encoding for voltage-gated K channel subunits underlying the neuronal M-current have been associated with infantile-onset epileptic disorders. The clinical spectrum ranges from self-limited neonatal seizures to epileptic e
Externí odkaz:
https://doaj.org/article/34faeeb0f7da4b4c958907783b71d468
Autor:
Suphalak Chokvithaya, Natarin Caengprasath, Aayalida Buasong, Supavadee Jantasuwan, Kanokwan Santawong, Netchanok Leela-adisorn, Siraprapa Tongkobpetch, Chupong Ittiwut, Vitchayaporn Saengow, Wuttichart Kamolvisit, Ponghatai Boonsimma, Saknan Bongsebandhu-Phubhakdi, Vorasuk Shotelersuk
Mutations in KCNQ2 encoding for voltage-gated K channel subunits underlying the neuronal M-current, have been associated with infantile-onset epileptic disorders. The clinical spectrum ranges from self-limited neonatal seizures to epileptic encephalo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::68f7b61e5694874ad03eb603ccc80588
https://doi.org/10.21203/rs.3.rs-1966853/v1
https://doi.org/10.21203/rs.3.rs-1966853/v1
Autor:
Ponthip Mekchay, Suwanna Muanpetch, Supang Maneesri le Grand, Chupong Ittiwut, Weerapan Khovidhunkit, Darintr Sosothikul, Benjaporn Akkawat, Rungnapa Ittiwut, Netchanok Leela-Adisorn, Ponlapat Rojnuckarin, Kanya Suphapeetiporn, Vorasuk Shotelersuk
Publikováno v:
Medicine
Hereditary thrombocytopenia comprises extremely diverse diseases that are difficult to diagnose by phenotypes alone. Definite diagnoses are helpful for patient (Pt) management. To evaluate the role of whole exome sequencing (WES) in these Pts. Cases