TYPE 2 GAUCHER DISEASE: ONSET AND EVOLUTION - CASE REPORT
Gaucher disease is the most common lysosomal storage disorder, with autosomal recessive transmission. The disease is due to glucocerebrosidase enzyme defi ciency, resulting in accumulation of glucocerebroside in all organs. The diagnosis is established by measuring enzyme activity. Among the clinica...
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Format: | Book |
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Amaltea Medical Publishing House,
2015-09-01T00:00:00Z.
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A1234.567 |
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Copy 1 | Available |