Genethon develops a promising drug to treat Duchenne muscular dystrophy
Duchenne disease treatment, dubbed "GNT0004", follows the principles of gene therapy. THE ESSENTIAL To help people with Duchenne muscular dystrophy, ...
Read moreDuchenne disease treatment, dubbed "GNT0004", follows the principles of gene therapy. THE ESSENTIAL To help people with Duchenne muscular dystrophy, ...
Read moreA first child has started to receive treatment as part of the gene therapy trial conducted by the Téléthon laboratory. ...
Read more© Getty ImagesDuchenne muscular dystrophy mainly affects boys.Duchenne muscular dystrophy is a rare disease that affects around 2,500 people in ...
Read moreScientific breakthrough! The CRISPR technique is based on the association of an RNA strand and an enzyme, once brought together, ...
Read more© Getty Images / Tetra images RFThe Duchenne muscular dystrophy is currently incurable. But a candidate treatment has just been ...
Read more© iStockPhotosA Franco-British team of researchers funded by Telethon donations has just discovered a promising gene therapy in the treatment ...
Read more© ThinkstockHow to treat the Duchenne muscular dystrophy, that fatal genetic disease that causes loss of muscle function? According to ...
Read more© istockAn advantage of 30 meters per year. Ataluren, from the American laboratory PTC Pharmaceuticals, which has just obtained temporary ...
Read moreIt is an incurable genetic disease, no treatment exists to cure this pathology. But a first child has received a ...
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