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Unbiased yeast screens identify cellular pathways affected in Niemann–Pick disease type C
Niemann–Pick disease type C (NPC) is a rare lysosomal storage disease caused by mutations in either the NPC1 or NPC2 genes. Mutations in the NPC1 gene lead to the majority of clinical cases (95%); however, the function of NPC1 remains unknown. To gain further insights into the biology of NPC1, we to...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | Life Sci Alliance |
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| Κύριοι συγγραφείς: | , , , , , , , , , , , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
Life Science Alliance LLC
2020
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7283134/ https://ncbi.nlm.nih.gov/pubmed/32487688 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.26508/lsa.201800253 |
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