https://www.drugdiscoverynews.com/the-past-present-and-future-of-gene-therapy-17093?utm_campaign=DDN_Newsletter_Dose&utm_medium=email&_hsenc=p2ANqtz--qJQp9C8hwBmdc2Juu_6IxiyDigzOykjTQ9BTDxzIVvn8FW9bYuuUkmWN_fI83eZ6u5eFPVPMeOtiMvboNN64Q_j8Tgg&_hsmi=418865587&utm_content=418865587&utm_source=hs_email
When Connie Elson was diagnosed with metachromatic leukodystrophy (MLD) at the age of five, her family had never heard of the disease. A rare inherited neurodegenerative disorder, MLD is caused by mutations in the ARSA (arylsulfatase A) gene, leading to a toxic build-up of sulfatides that progressively destroy the nervous system.
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