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Published in 2022 at "Frontiers in Cell and Developmental Biology"
DOI: 10.3389/fcell.2022.902969
Abstract: Background: NGLY1 is an enigmatic enzyme with multiple functions across a wide range of species. In humans, pathogenic genetic variants in NGLY1 are linked to a variable phenotype of global neurological dysfunction, abnormal tear production,…
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Keywords:
nervous musculoskeletal;
ngly1 deficiency;
zebrafish model;
deficiency ... See more keywords