Orawan Iamopas

Whole exome sequencing revealed mutations in FBXL4, UNC80, and ADK in Thai patients with severe intellectual disabilities.

C. Srichomthong, K. Suphapeetiporn, V. Shotelersuk, 2019, Gene.

Two infants with abetalipoproteinemia: Classic versus atypical presentation

D. Wattanasirichaigoon, P. Tanpowpong, S. Treepongkaruna, 2019, Pediatrics International.