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The impact of Megf10/Drpr gain-of-function on muscle development in Drosophila
Recessive mutations in multiple EGF-like domains 10 (MEGF10) underlie a rare congenital muscle disease known as MEGF10 myopathy. MEGF10 and its Drosophila homolog Draper (Drpr) are transmembrane receptors expressed in muscle and glia. Drpr deficiency is known to result in muscle abnormalities in fli...
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| Publicat a: | FEBS Lett |
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| Autors principals: | , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2019
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6504253/ https://ncbi.nlm.nih.gov/pubmed/30802937 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/1873-3468.13348 |
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