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Published in 2019 at "Blood"
DOI: 10.1182/blood-2019-128143
Abstract: Gaucher Disease (GD) is an autosomal recessive metabolic disorder due to glucocerebrosidase deficit. There are three main clinical phenotypes: type I (GD1: non-neuronopathic form), characterized by a visceral involvement that can mimic a hematologic disease;…
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Keywords:
gd1;
patients gd1;
gd1 patients;
gd1 gd3 ... See more keywords