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Jung-Min Ko, Ph.D. - Publications

Affiliations: 
2001 University of Texas at Austin, Austin, Texas, U.S.A. 
Area:
Bilingual and Multicultural Education, Speech Communication, Adult and Continuing Education
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9 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2018 Kim D, Ko JM, Kim YM, Seo GH, Kim GH, Lee BH, Yoo HW. Low prevalence of argininosuccinate lyase deficiency among inherited urea cycle disorders in Korea. Journal of Human Genetics. PMID 29773863 DOI: 10.1038/s10038-018-0467-2  0.414
2018 Kim YM, Seo GH, Kim GH, Ko JM, Choi JH, Yoo HW. 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. PMID 29506479 DOI: 10.1186/s12881-018-0546-4  0.37
2017 Choi JH, Lee BH, Heo SH, Kim GH, Kim YM, Kim DS, Ko JM, Sohn YB, Hong YH, Lee DH, Kook H, Lim HH, Kim KH, Kim WS, Hong GR, et al. 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. PMID 28723748 DOI: 10.1097/MD.0000000000007387  0.41
2016 Yoo H, Ko JM, Lim BC, Cheong HI. First Korean Patients with Craniofrontonasal Syndrome Confirmed by EFNB1 Analysis. Annals of Clinical and Laboratory Science. 46: 544-548. PMID 27650623  0.438
2016 Kim YM, Cheon CK, Park KH, Park S, Kim GH, Yoo HW, Lee KA, Ko JM. 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. PMID 27466294  0.412
2016 Myeong J, Ko J, Hong C, Yang D, Lee KP, Jeon JH, So I. The interaction domains of transient receptor potential canonical (TRPC)1/4 and TRPC1/5 heteromultimeric channels. Biochemical and Biophysical Research Communications. PMID 27131740 DOI: 10.1016/J.Bbrc.2016.04.138  0.38
2016 Choi JS, Yoo HW, Lee KJ, Ko JM, Moon JS, Ko JS. 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. PMID 27066452 DOI: 10.5223/pghn.2016.19.1.76  0.375
2016 Kim SH, Lee NE, Lee JS, Shin JH, Lee JY, Ko JH, Chang CL, Kim YS. Identification of mycobacterial antigens in human urine using immunoglobulin G isolated from sera of patients with active pulmonary tuberculosis. Journal of Clinical Microbiology. PMID 26984972 DOI: 10.1128/JCM.00236-16  0.441
2016 Ko JM, Seo J, Choi M, Song J, Lee KA, Shin CH. 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. PMID 26927351  0.303
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