Browsing by Author Lee, HCH

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TitleAuthor(s)Issue DateViews
 
2020
18
 
2012
205
 
2010
146
 
2020
35
 
The KLHL40C.1516A>C is a Chinese-specific founder mutation in causing nemaline myopathy 8
Proceeding/Conference:Joint Annual Scientific Meeting 2019 of The Hong Kong Paediatric Society, Hong Kong College of Paediatricians, Hong Kong Paediatric Nurses Association, & Hong Kong College of Paediatric Nursing
2019
26