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Molecular Cell|February 20, 1999
Altered trafficking of lysosomal proteins in Hermansky-Pudlak syndrome due to mutations in the beta 3A subunit of the AP-3 adaptorE C Dell'Angelica, V Shotelersuk, R C Aguilar, et al.The Southeast Asian Journal of Tropical Medicine and Public Health|September 15, 2001
Clinical and molecular characteristics of Thai patients with achondroplasiaV Shotelersuk, C Ittiwut, S Srivuthana, et al.Scandinavian Journal of Immunology|October 5, 2012
Clinical and molecular characterization of Thai patients with Wiskott-Aldrich syndromeP Amarinthnukrowh, S Ittiporn, S Tongkobpetch, et al.American Journal of Medical Genetics|March 3, 1998
Normal brain myelination in a patient homozygous for a mutation that encodes a severely truncated methionine adenosyltransferase I/IIIS Hazelwood, I Bernardini, V Shotelersuk, et al.The Southeast Asian Journal of Tropical Medicine and Public Health|April 6, 2001
Establishing gas chromatography-mass spectrometry to diagnose organic acidemias in ThailandV Shotelersuk, S Srivuthana, S Wacharasindhu, et al.Molecular Genetics and Metabolism|March 9, 1999
Identification and detection of the common 65-kb deletion breakpoint in the nephropathic cystinosis gene (CTNS)Y Anikster, C Lucero, J W Touchman, et al.American Journal of Human Genetics|October 30, 1998
CTNS mutations in an American-based population of cystinosis patientsV Shotelersuk, D Larson, Y Anikster, et al.Molecular Genetics and Metabolism|August 15, 1998
Three new mutations in a gene causing Hermansky-Pudlak syndrome: clinical correlationsV Shotelersuk, S Hazelwood, D Larson, et al.Journal of Endocrinological Investigation|February 6, 2008
Two common and three novel PDS mutations in Thai patients with Pendred syndromeT Snabboon, W Plengpanich, S Saengpanich, et al.Molecular Genetics and Metabolism|November 16, 2001
CTNS mutations in African American patients with cystinosisR Kleta, Y Anikster, C Lucero, et al.Pageof 5