Article Versions Notes

Klangjorhor J, Wiwattanadittakul N, Jaimalai T, Thongkumkoon P, Noisagul P, Khiaomai R, Sirikaew N, Moonsan N, Pasena A, Suksakit P, et al. A Novel Homozygous Missense Variant of PIGT Related to Multiple Congenital Anomalies-Hypotonia Seizures Syndrome 3 with Elevated of Serum ALP Level in a Thai Newborn Patient. International Journal of Molecular Sciences. 2025; 26(6):2790. https://doi.org/10.3390/ijms26062790

Klangjorhor, Jeerawan, Natrujee Wiwattanadittakul, Thanapak Jaimalai, Patcharawadee Thongkumkoon, Pitiporn Noisagul, Ratchadaporn Khiaomai, Nutnicha Sirikaew, Nonthanan Moonsan, Arnat Pasena, Pathacha Suksakit, and et al. 2025. "A Novel Homozygous Missense Variant of PIGT Related to Multiple Congenital Anomalies-Hypotonia Seizures Syndrome 3 with Elevated of Serum ALP Level in a Thai Newborn Patient" International Journal of Molecular Sciences 26, no. 6: 2790. https://doi.org/10.3390/ijms26062790

Klangjorhor, J., Wiwattanadittakul, N., Jaimalai, T., Thongkumkoon, P., Noisagul, P., Khiaomai, R., Sirikaew, N., Moonsan, N., Pasena, A., Suksakit, P., Teeyakasem, P., Chaiyawat, P., & Tengsujaritkul, M. (2025). A Novel Homozygous Missense Variant of PIGT Related to Multiple Congenital Anomalies-Hypotonia Seizures Syndrome 3 with Elevated of Serum ALP Level in a Thai Newborn Patient. International Journal of Molecular Sciences, 26(6), 2790. https://doi.org/10.3390/ijms26062790