Nithiwat Vatanavicharn
4PUBLICATIONS
8CO-AUTHORS
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Publications (4)
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|Jun 27, 2024
Homozygosity for a Rare Plec Variant Suggests a Contributory Role in Congenital Insensitivity to Pain.Piranit Kantaputra, Teerada Daroontum, Kantapong Kitiyamas
|Dec 13, 2022
Multisuture craniosynostosis: a case report of unusual presentation of chromosome 14q32 deletion.Sarut Chaisrisawadisuk, Nithiwat Vatanavicharn, Inthira Khampalikit
|Nov 02, 2022
Phenotypic and molecular features of Thai patients with primary carnitine deficiency.Somporn Liammongkolkul, Boonchai Boonyawat, Chodchanok Vijarnsorn
|Mar 07, 2021
Molecular characterization of Thai patients with phenylalanine hydroxylase deficiency and in vitro functional study of two novel PAH variants.Lukana Ngiwsara, Nithiwat Vatanavicharn, Phannee Sawangareetrakul
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