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Molecular Medicine Reports|December 9, 2014
A family with axonal sensorimotor polyneuropathy with TUBB3 mutationYoung Bin Hong, Ja Hyun Lee, Hyung Jun Park, et al.
Molecular Medicine Reports|May 7, 2016
Recessive optic atrophy, sensorimotor neuropathy and cataract associated with novel compound heterozygous mutations in OPA1Jinho Lee, Sung-Chul Jung, Young Bin Hong, et al.
European Archives of Oto-Rhino-Laryngology : Official Journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : Affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery|January 5, 2008
A polyethylene glycol grafted bi-layered polyurethane scaffold: preliminary study of a new candidate prosthesis for repair of a partial tracheal defectHong-Shik Choi, Hwal Suh, Ja-Hyun Lee, et al.
BMC Medical Genetics|December 10, 2013
A compound heterozygous mutation in HADHB gene causes an axonal Charcot-Marie-tooth diseaseYoung Bin Hong, Ja Hyun Lee, Jin-Mo Park, et al.
BMC Neurology|October 7, 2015
A novel homozygous MPV17 mutation in two families with axonal sensorimotor polyneuropathyYu-Ri Choi, Young Bin Hong, Sung-Chul Jung, et al.
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