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아주대학교 의학문헌정보센터
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Browsing "Medical Genetics" by Journal : Orphanet journal of rare diseases
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Showing results 4 to 6 of 6
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2013
Phase I/II clinical trial of enzyme replacement therapy with idursulfase beta in patients with mucopolysaccharidosis II (Hunter syndrome).
손영배
2020
The GBA p.G85E mutation in Korean patients with non-neuronopathic Gaucher disease: founder and neuroprotective effects
손영배
2022
The Korean undiagnosed diseases program phase I: expansion of the nationwide network and the development of long-term infrastructure
손영배
1
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아주대학교 의학문헌정보센터
