Search Results - Cheon, Chong Kun, MD

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  1. 1
    OTC Gene in Ornithine Transcarbamylase Deficiency: Clinical Course and Mutational Spectrum in Seven Korean Patients

    OTC Gene in Ornithine Transcarbamylase Deficiency: Clinical Course and Mutational Spectrum in Seven Korean Patients by Lee, Jung Hyun, MD, Kim, Gu-Hwan, PhD, Yoo, Han-Wook, MD, Cheon, Chong-Kun, MD

    Published in Pediatric neurology
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  2. 2
    Melkersson-Rosenthal Syndrome With Hashimoto Thyroiditis in a 9-Year-Old Girl: An Autoimmune Disorder

    Melkersson-Rosenthal Syndrome With Hashimoto Thyroiditis in a 9-Year-Old Girl: An Autoimmune Disorder by Lee, Yun-Jin, MD, PhD, Cheon, Chong Kun, MD, PhD, Yeon, Gyu Min, MD, Kim, Young Mi, MD, PhD, Nam, Sang Ook, MD, PhD

    Published in Pediatric neurology
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  3. 3
    Novel Mutation in SLC6A19 Causing Late-Onset Seizures in Hartnup Disorder

    Novel Mutation in SLC6A19 Causing Late-Onset Seizures in Hartnup Disorder by Cheon, Chong Kun, MD, Lee, Beom Hee, MD, Ko, Jung Min, MD, Kim, Hyun-Ji, MD, Yoo, Han-Wook, MD

    Published in Pediatric neurology
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