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Haemostatic abnormalities and lupus anticoagulant activity in patients with Gaucher disease type I

โœ Scribed by R. Barone; G. Giuffrida; R. Musso; G. Carpinteri; A. Fiumara


Book ID
110226882
Publisher
Springer
Year
2000
Tongue
English
Weight
50 KB
Volume
23
Category
Article
ISSN
0141-8955

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## Communicated by Mark Paalman Gaucher disease, the most common lysosomal storage disorder, results from the inherited deficiency of the enzyme glucocerebrosidase. Three clinical types are recognized: type 1, nonneuronopathic; type 2, acute neuronopathic; and type 3, subacute neuronopathic. Type 2