J. Hwang

发表

Inheritance of Charcot–Marie–Tooth disease 1A with rare nonrecurrent genomic rearrangement

N. Kim, H. Jeon, Byung-Ok Choi, 2011, neurogenetics.

Lower Leg MRI Features in Axonal Charcot-Marie-Tooth Patients with MFN2 Mutations

Byung-Ok Choi, B. Suh, D. Shim, 2007 .

Kearns-Sayre Syndrome with a Large Deletion in Mitochondrial DNA

Byung-Ok Choi, S. Kim, Hee-Jin Kim, 2006 .

X-linked Charcot-Marie-Tooth Patient with a Novel Cys168Arg Missense Mutation in the Connexin32 Gene.

Byung-Ok Choi, J. Hwang, K. Chung, 2004 .

Rapid diagnosis of CMT1A duplications and HNPP deletions by multiplex microsatellite PCR.

Byung-Ok Choi, Joonki Kim, J. Hwang, 2007, Molecules and cells.

Genetic Kinship and Discrimination between the Cultivars Consisting a Sister Cultivar Group in Spring Orchid Cymbidium goeringii

Kyung Suk Lee, J. Hwang, K. Chung, 2021 .

Mutational analysis of whole mitochondrial DNA in patients with MELAS and MERRF diseases

K. Seong, H. Jeon, Byung-Ok Choi, 2010, Experimental & Molecular Medicine.

Mutational analysis of PMP22, MPZ, GJB1, EGR2 and NEFL in Korean Charcot‐Marie‐Tooth neuropathy patients

Byung-Ok Choi, J. Hwang, K. Chung, 2004, Human mutation.

Compound heterozygous mutations of TYMP as underlying causes of mitochondrial neurogastrointestinal encephalomyopathy (MNGIE).

Ji Hoon Park, H. Kim, Byung-Ok Choi, 2013, Molecular medicine reports.

Compound mutations of PEO1 and TYMP in a progressive external ophthalmoplegia patient with incomplete mitochondrial neurogastrointestinal encephalomyopathy phenotype

Byung-Ok Choi, Sun Wha Park, J. Hwang, 2011, Genes & Genomics.

Early onset severe and late-onset mild Charcot-Marie-Tooth disease with mitofusin 2 (MFN2) mutations.

J. Hwang, K. Chung, J. Suh, 2006, Brain : a journal of neurology.

A MELAS syndrome family harboring two mutations in mitochondrial genome

Byung-Ok Choi, Joonki Kim, Hyang-Woon Lee, 2008, Experimental & Molecular Medicine.

Genetic polymorphisms of eight X-STR loci of Mentype Argus X-8 kit in Koreans

Sun Wha Park, J. Hwang, K. Chung, 2011 .

Compound heterozygous mutations of TYMP as underlying causes of mitochondrial neurogastrointestinal encephalomyopathy (MNGIE).

Ji Hoon Park, Byung-Ok Choi, B. Suh, 2013, Molecular medicine reports.