Jinho Lee

发表

Charcot‐Marie‐Tooth Disease Type 4H Resulting from Compound Heterozygous Mutations in FGD4 from Nonconsanguineous Korean Families

Deok‐Ho Kim, H. Koo, H. Kim, 2015, Annals of human genetics.

Overexpression of mutant HSP27 causes axonal neuropathy in mice

G. Kwak, Byung-Ok Choi, Y. Hong, 2015, Journal of Biomedical Science.

ADSSL1 mutation relevant to autosomal recessive adolescent onset distal myopathy

Ji Eun Lee, H. Kim, Won Min Mo, 2016, Annals of neurology.

DGAT2 Mutation in a Family with Autosomal‐Dominant Early‐Onset Axonal Charcot‐Marie‐Tooth Disease

J. Kim, Ji Eun Lee, H. Koo, 2016, Human mutation.

Development of cell models for high-throughput screening system of Charcot-Marie-Tooth disease type 1

Byung-Ok Choi, Y. Hong, S. Yoo, 2015 .

Recessive optic atrophy, sensorimotor neuropathy and cataract associated with novel compound heterozygous mutations in OPA1

H. Koo, Byung-Ok Choi, Y. Hong, 2016, Molecular medicine reports.

Overexpression of mutant HSP27 causes axonal neuropathy in mice

G. Kwak, Byung-Ok Choi, Y. Hong, 2015, Journal of Biomedical Science.

Severe phenotypes in a Charcot–Marie–Tooth 1A patient with PMP22 triplication

Byung-Ok Choi, K. Chung, Jinho Lee, 2014, Journal of Human Genetics.

Ser135Phe mutation in HSPB1 (HSP27) from Charcot–Marie–Tooth disease type 2F families

H. Kim, Byung-Ok Choi, Y. Hong, 2015, Genes & Genomics.

A novel homozygous MPV17 mutation in two families with axonal sensorimotor polyneuropathy

H. Koo, Byung-Ok Choi, Y. Hong, 2015, BMC Neurology.

Dynamic Transcriptional Events in Distal Sural Nerve Revealed by Transcriptome Analysis

Byung-Ok Choi, Y. Hong, H. Moon, 2014, Experimental neurobiology.