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Twiitti käyttäjältä @amchelsinki

Julkaistu 10.09.2020 klo 13:59

A new discovery shows how mutations in a novel gene, ANGPT2, cause primary lymphedema. This opens possibilities for the development of improved treatments of the disease. @helsinkiuni #HelsinkiHealth https://t.co/YSMNm3cgDO

— Academic Medical Center Helsinki (@amchelsinki) September 10, 2020 10:59
Asiasanat HelsinkiHealth
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