ノバルティスのインスタグラム(novartis) - 2月5日 17時00分

Matteo, 4, was born with a rare genetic disease that leads to progressive muscle weakness. Untreated, infants with the severest form often don’t live beyond age 2. Matteo received a gene therapy when he was just 27 days old.
Click the link in our Bio to learn more about the over 20,000 dedicated researchers contribute to our pipeline of serious disease therapies with the potential to have a significant impact on lives.

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