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Researchers study gene transporter to treat haemophilia
Haemophilia A is a rare genetic disorder in which blood does not clot properly. NCCS scientists are studying the use of cord-lining stem cells to transport a specific gene into the body that will then go on to producing a clotting protein known as factor VIII, which patients lack.
 

 

Multinational study reveals titin gene mutations affect heart function in healthy individuals

 

 

  

SERI research on efficacy of acupuncture and diet to treat dry eye

 

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In-depth study of lung cancer mutations in Singapore patients