Clinical and genetic characteristics of Korean patients with IARS2-related disorders
Author(s) -
Jin Sook Lee,
Man Jin Kim,
Soo Yeon Kim,
Byung Chan Lim,
Ki Joong Kim,
Murim Choi,
MoonWoo Seong,
JongHee Chae
Publication year - 2019
Publication title -
journal of genetic medicine
Language(s) - English
Resource type - Journals
eISSN - 2233-9108
pISSN - 1226-1769
DOI - 10.5734/jgm.2019.16.2.55
Subject(s) - cataracts , genetics , phenotype , mitochondrial disease , hearing loss , biology , sensorineural hearing loss , compound heterozygosity , transfer rna , mitochondrial dna , medicine , gene , audiology , rna
Jin Sook Lee , Man Jin Kim , Soo Yeon Kim , Byung Chan Lim , Ki Joong Kim , Murim Choi , Moon-Woo Seong , and Jong-Hee Chae* Department of Pediatrics, Gachon University Gil Medical Center, Gachon University College of Medicine, Incheon, Korea Department of Laboratory Medicine, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Korea Department of Pediatrics, Pediatric Clinical Neuroscience Center, Seoul National University Children’s Hospital, Seoul National University College of Medicine, Seoul, Korea Department of Biomedical Sciences, Seoul National University College of Medicine, Seoul, Korea
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