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CASK Mutation in an Infant with Microcephaly, Pontocerebellar Hypoplasia, and Hearing Loss
Jun Chul Byun, Jung Sook Ha
Ann Child Neurol. 2022;30(4):216-219.   Published online September 22, 2022
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A Case of Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease with Acute Bilateral Total Blindness
Jiyoon Ko, Ji-Hoon Na, Hyunjoo Lee, Jun Chul Byun, Joon Sik Kim, Young-Mock Lee
Ann Child Neurol. 2022;30(4):197-200.   Published online September 8, 2022
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TSEN54 Gene-Related Pontocerebellar Hypoplasia Type 2 in a Newborn with Refractory Myoclonic Seizures
Jun Chul Byun, Jung Sook Ha, Chun Soo Kim
Ann Child Neurol. 2022;30(3):152-154.   Published online June 28, 2022
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A SERPINC1 Mutation in a Patient with Cerebral Venous Thrombosis and Upper-Extremity Deep Vein Thrombosis
Jun Chul Byun, Jeong-Ho Hong
Ann Child Neurol. 2022;30(3):134-136.   Published online May 25, 2022
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Clinical Characteristics of Epilepsy and Its Risk Factors in Neurofibromatosis Type 1: A Single-Center Study
Areum Shin, Jun Chul Byun, Su-Kyeong Hwang, Soonhak Kwon, Yun Jeong Lee
Ann Child Neurol. 2021;29(1):1-7.   Published online December 28, 2020
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