Gaucher's disease with uncommon presentations

Gaucher's disease is the most common lysosomal storage disorder gene defect, which leads to deficiency or decreased activity of glucocerebrosidase, followed by accumulation of glucosylceramide. There is autosomal recessive transmission leading to varied clinical manifestations. This disease has...

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Kaydedildi:
Detaylı Bibliyografya
Asıl Yazarlar: Gupta, Sanjay Sen, Mondal, Palash, Basu, Nandita, Mallick, Mamata Guha
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Medknow Publications Pvt Ltd 2009
Konular:
Case Report
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC3168013/
https://ncbi.nlm.nih.gov/pubmed/21938170
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0970-9371.59399
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