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Skin Ultrastructural Findings in Type 2 Gaucher Disease: Diagnostic Implications
BACKGROUND: Type 2 Gaucher disease is a rare and progressive subtype of this lysosomal storage disorder, marked by rapid, early-onset neurodegeneration. Distinguishing type 2 from types 1 and 3 Gaucher disease has remained challenging, due to the lack of a clear correlation between phenotype and enz...
Αποθηκεύτηκε σε:
| Κύριοι συγγραφείς: | , , , , , , , , , |
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| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
2011
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3224209/ https://ncbi.nlm.nih.gov/pubmed/21982627 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ymgme.2011.09.008 |
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