Molecular basis and diagnosis of thalassemia

por Lee, Jee-Soo, Cho, Sung Im, Park, Sung Sup, Seong, Moon-Woo
Publicado 2021

Skewed X-Chromosome Inactivation in a Korean Girl with Severe Mucopolysaccharidosis Type II

por Kim, Hwa Young, Kim, Man Jin, Seong, Moon-Woo, Ko, Jung Min
Publicado 2022

Association of Tandem Repeat Number Variabilities in Subunit S of the Type I Restriction-Modification System with Macrolide Resistance in Mycoplasma pneumoniae

por Lee, Joon-Kee, Seong, Moon-Woo, Yun, Ki-Wook, Choi, Eun-Hwa
Publicado 2022

Frequency and clinical implications of the isolation of rare nontuberculous mycobacteria

por Kim, Junghyun, Seong, Moon-Woo, Kim, Eui-Chong, Han, Sung Koo, Yim, Jae-Joon
Publicado 2015

Genotypic profile and phenotype correlations of ABCA4-associated retinopathy in Koreans

por Joo, Kwangsic, Seong, Moon-Woo, Park, Kyu Hyung, Park, Sung Sup, Woo, Se Joon
Publicado 2019

Neonatal invasive Streptococcus gallolyticus subsp. pasteurianus infection with delayed central nervous system complications

por Park, Jung-Weon, Eun, So-Hee, Kim, Eui-Chong, Seong, Moon-Woo, Kim, Yun-Kyung
Publicado 2015

Bietti Crystalline Retinopathy Confirmed by Mutation of CYP4V2 Gene in a Korean Patient

por Park, Young Joo, Hwang, Duck Jin, Seong, Moon-Woo, Park, Sung Sup, Woo, Se Joon
Publicado 2016

Retinitis Pigmentosa Associated with Bardet-Biedl Syndrome with BBS9 Gene Mutation in a Korean Patient

por Kim, Yong Hoon, Joo, Kwang Sic, Seong, Moon-Woo, Park, Sung Sup, Woo, Se Joon
Publicado 2020

Two Cases of Facioscapulohumeral Muscular Dystrophy 2 in Korea

por Lee, Jung Hwan, Park, Hyung Jun, Seong, Moon-Woo, Park, Sung Sup, Choi, Young-Chul
Publicado 2021

Genetic mutation spectrum of pantothenate kinase-associated neurodegeneration expanded by breakpoint sequencing in pantothenate kinase 2 gene

por Yang, Dahae, Cho, Sanghyun, Cho, Sung Im, Kim, Manjin, Seong, Moon-Woo, Park, Sung Sup
Publicado 2022

Progressive Cognitive and Behavioral Changes With Leukodystrophy due to ABCD1 Gene Mutation

por Park, Jinseok, Lee, Sanggon, Lee, Heerah, Lee, Jee Soo, Seong, Moon-Woo, Kim, Hee-Jin
Publicado 2022

The First Study on Nucleotide-level Identification of Hb Koriyama in a Patient with Severe Hemolytic Anemia

por Park, Seungman, Park, Jun Eun, Cho, Sung Im, Jeon, Yongbum, Park, Sung Sup, Seong, Moon-Woo
Publicado 2012

Clinical and genetic spectrum of GSD type 6 in Korea

por Hahn, Jong Woo, Lee, Heerah, Seong, Moon Woo, Kang, Gyeong Hoon, Moon, Jin Soo, Ko, Jae Sung
Publicado 2023

The First Korean Case of Lysinuric Protein Intolerance: Presented with Short Stature and Increased Somnolence

por Ko, Jung Min, Shin, Choong Ho, Yang, Sei Won, Seong, Moon Woo, Park, Sung Sup, Song, Junghan
Publicado 2012

Comparison of 3 Automated Immunoassays for Detection of Anti-Hepatitis A Virus Immunoglobulin M in a Tertiary Care Hospital

por Park, Hyewon, Lee, Yu-joo, Seong, Moon-Woo, Lee, Do-Hoon, Park, Myoung Hee, Song, Eun Young
Publicado 2013

Analytical and Clinical Validation of Six Commercial Middle East Respiratory Syndrome Coronavirus RNA Detection Kits Based on Real-Time Reverse-Transcription PCR

por Kim, Mi-Na, Ko, Young Jin, Seong, Moon-Woo, Kim, Jae-Seok, Shin, Bo-Moon, Sung, Heungsup
Publicado 2016

Cardiomyopathies with Mixed and Inapparent Morphological Features in Cardiac Troponin I3 Mutation

por Sohn, Dae-Won, Kim, Hyung-Kwan, Kim, Yong-Jin, Oh, Seil, Seong, Moon-Woo, Park, Sung-Sup
Publicado 2017

Erratum: Cardiomyopathies with Mixed and Inapparent Morphological Features in Cardiac Troponin I3 Mutation

por Sohn, Dae-Won, Kim, Hyung-Kwan, Kim, Yong-Jin, Oh, Seil, Seong, Moon-Woo, Park, Sung-Sup
Publicado 2017

Congenital Stationary Night Blindness due to Novel TRPM1 Gene Mutations in a Korean Patient

por Lee, Yun Jeong, Joo, Kwangsic, Seong, Moon-Woo, Park, Kyu Hyung, Park, Sung Sup, Woo, Se Joon
Publicado 2020

Molecular characterization of Leber congenital amaurosis in Koreans

por Seong, Moon-Woo, Kim, Seong Yeon, Yu, Young Suk, Hwang, Jeong-Min, Kim, Ji Yeon, Park, Sung Sup
Publicado 2008