טוען...
Silencing of drpr Leads to Muscle and Brain Degeneration in Adult Drosophila
Mutations in the gene encoding the single transmembrane receptor multiple epidermal growth factor-like domain 10 (MEGF10) cause an autosomal recessive congenital muscle disease in humans. Although mammalian MEGF10 is expressed in the central nervous system as well as in skeletal muscle, patients car...
שמור ב:
| Main Authors: | , , , , , |
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| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
American Society for Investigative Pathology
2014
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4188861/ https://ncbi.nlm.nih.gov/pubmed/25111228 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ajpath.2014.06.018 |
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