Jung-Min Ko, Ph.D.
Affiliations: | 2001 | University of Texas at Austin, Austin, Texas, U.S.A. |
Area:
Bilingual and Multicultural Education, Speech Communication, Adult and Continuing EducationGoogle:
"Jung-Min Ko"Mean distance: 3010.31
Parents
Sign in to add mentor| Diane L. Schallert | grad student | 2001 | UT Austin | |
| (The effect of negotiation of meaning on the storytelling of adult students in ESL classrooms.) | ||||
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Publications
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| Kim D, Ko JM, Kim YM, et al. (2018) Low prevalence of argininosuccinate lyase deficiency among inherited urea cycle disorders in Korea. Journal of Human Genetics |
| Kim YM, Seo GH, Kim GH, et al. (2018) A case of an infant suspected as IMAGE syndrome who were finally diagnosed with MIRAGE syndrome by targeted Mendelian exome sequencing. Bmc Medical Genetics. 19: 35 |
| Choi JH, Lee BH, Heo SH, et al. (2017) Clinical characteristics and mutation spectrum of GLA in Korean patients with Fabry disease by a nationwide survey: Underdiagnosis of late-onset phenotype. Medicine. 96: e7387 |
| Yoo H, Ko JM, Lim BC, et al. (2016) First Korean Patients with Craniofrontonasal Syndrome Confirmed by EFNB1 Analysis. Annals of Clinical and Laboratory Science. 46: 544-548 |
| Kim YM, Cheon CK, Park KH, et al. (2016) Novel and Recurrent ACADS Mutations and Clinical Manifestations Observed in Korean Patients with Short-chain Acyl-coenzyme a Dehydrogenase Deficiency. Annals of Clinical and Laboratory Science. 46: 360-6 |
| Myeong J, Ko J, Hong C, et al. (2016) The interaction domains of transient receptor potential canonical (TRPC)1/4 and TRPC1/5 heteromultimeric channels. Biochemical and Biophysical Research Communications |
| Choi JS, Yoo HW, Lee KJ, et al. (2016) Novel Mutations in the CPT1A Gene Identified in the Patient Presenting Jaundice as the First Manifestation of Carnitine Palmitoyltransferase 1A Deficiency. Pediatric Gastroenterology, Hepatology & Nutrition. 19: 76-81 |
| Kim SH, Lee NE, Lee JS, et al. (2016) Identification of mycobacterial antigens in human urine using immunoglobulin G isolated from sera of patients with active pulmonary tuberculosis. Journal of Clinical Microbiology |
| Ko JM, Seo J, Choi M, et al. (2016) Rare Korean Cases of Very-long-chain Acyl-CoA Dehydrogenase Deficiency with a Novel Recurrent Mutation. Annals of Clinical and Laboratory Science. 46: 97-101 |