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Generation and characterization of NGLY1 patient-derived midbrain organoids https://t.co/rmxmglRLHu
Generation and characterization of NGLY1 patient-derived midbrain organoids https://t.co/rmxmglRLHu
RT @FrontCellDevBio: New Research: Generation and characterization of NGLY1 patient-derived midbrain organoids: NGLY1 deficiency is an ultr…
New Research: Generation and characterization of NGLY1 patient-derived midbrain organoids: NGLY1 deficiency is an ultra-rare, autosomal recessive genetic disease caused by mutations in the NGLY1 gene encoding N-glycanase one that removes… https://t.co/W1yT