Ann Lab Med 2018; 38(1): 80-82  
Identification of Homozygous Likely Pathogenic Variant of ALDH3A2 in a Korean Boy with Sjögren–Larsson Syndrome
Je Yeon Kim, M.D.1, Shin-Hye Kim, M.D.1, Mi-Jung Park, M.D.1, Soung Hee Kim, M.D.2, Woo Ho Cho, M.D.2, Jin Choi, M.D.3, Chang-Seok Ki, M.D.4, and Su Jeong You, M.D.1
Department of Pediatrics1, Inje University Sanggye Paik Hospital, Inje University College of Medicine, Seoul; Department of Radiology2, Inje University Sanggye Paik Hospital, Inje University College of Medicine, Seoul; Department of Ophthalmology3, Inje University Sanggye Paik Hospital, Inje University College of Medicine, Seoul; Department of Laboratory Medicine and Genetics4, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea
Correspondence to: Chang-Seok Ki
Department of Laboratory Medicine and Genetics, Samsung Medical Center, 81 Irwon-ro, Gangnam-gu, Seoul 06351, Korea
Tel: +82-2-3410-2709, Fax: +82-2-3410-2719, E-mail: changski@skku.edu
Co-Corresponding author: Su Jeong You
Department of Pediatrics, Inje University Sanggye Paik Hospital, Inje University College of Medicine, 1342 Dongil-ro, Nowon-gu, Seoul 01757, Korea
Tel: + 82-2-950-1080, Fax: +82-2-951-1246, E-mail: sjyou@paik.ac.kr.or
Received: January 23, 2017; Revised: June 1, 2017; Accepted: September 16, 2017; Published online: January 1, 2018.
© The Korean Society for Laboratory Medicine. All rights reserved.

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