Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Haesoo Koo"'
Autor:
Young Bin Hong, Jee Young Kim, Jin Seok Yu, Kee Duk Park, Byung Ok Choi, Ki Wha Chung, Haesoo Koo, Sun Sung Choi
Publikováno v:
Genes & Genomics. 38:659-667
Charcot-Marie-Tooth disease type 1E (CMT1E) is a demyelinating motor and sensory neuropathy with peripheral myelin protein 22 (PMP22) point mutations. The objective of this study was to identify genetic causes and determine genotype–phenotype corre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9ba6d7bc1ad4d375a72ff8e4f98716f3
https://doi.org/10.1007/s13258-016-0423-5
https://doi.org/10.1007/s13258-016-0423-5
Autor:
Byung Ok Chot, Young Bin Hong, Haesoo Koo, Kee Duk Park, Ji Young Park, Jee Young Kim, Sung Hee Kim, Ki Wha Chung
Publikováno v:
Neurology India. 65:893
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9e9f089d93f8e0bd52ce71e7d13d79ed
https://doi.org/10.4103/neuroindia.ni_783_16
https://doi.org/10.4103/neuroindia.ni_783_16
Publikováno v:
Journal of the Korean Association of Pediatric Surgeons. 18:83
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f3f915ede9288f4b65aad6a2eaa1e5ec
https://doi.org/10.13029/jkaps.2012.18.2.83
https://doi.org/10.13029/jkaps.2012.18.2.83
Autor:
Jee Young Kim, Sung-Hee Kim, Ji-Young Park, Haesoo Koo, Kee-Duk Park, Young Bin Hong, Ki Wha Chung, Byung-Ok Chot
Publikováno v:
Neurology India; Jul/Aug2017, Vol. 65 Issue 4, p893-895, 3p
Publikováno v:
Journal of the Korean Radiological Society. 43:629
Fukuyama congenital muscular dystrophy is a genetic disease and common in Japan. The typical clinical features are hypotonia with an early infantile onset and severe developmental delay. The diagnosis is based on pathologic evidence of muscular dystr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e546349eeb43c456292b36b67cc91e78
https://doi.org/10.3348/jkrs.2000.43.5.629
https://doi.org/10.3348/jkrs.2000.43.5.629