Whole-exome sequencing reveals a novel COL2A1 mutation in a patient with spondyloepiphyseal dysplasia congenita

by A. Sangsin, C. Srichomthong, M. Pongpanich, K. Suphapeetiporn, V. Shotelersuk
Published 2018

Whole genome sequencing identifies a homozygous nonsense mutation in the JPH2 gene in Shih Tzu dogs with progressive retinal atrophy

by G. Urkasemsin, M. Pongpanich, L. Sariya, A. Kongcharoen, R. Buddhirongawatr, S. Rungarunlert, J. N. Ferreira, W. Chetruengchai, C. Phokaew, C. Srichomthong, V. Shotelersuk
Published 2022