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Published in 2020 at "Molecular genetics and metabolism"
DOI: 10.1016/j.ymgme.2020.07.011
Abstract: Gaucher disease (GD) is caused by pathogenic mutations in GBA1, the gene that encodes the lysosomal enzyme β-glucocerebrosidase. Despite the existence of a variety of specific treatments for GD, they cannot completely reverse bone complications.…
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Keywords:
unraveling mystery;
density;
bone;
mystery gaucher ... See more keywords