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Dystrophin Dp71 and the Neuropathophysiology of Duchenne Muscular Dystrophy
Duchenne muscular dystrophy (DMD) is caused by frameshift mutations in the DMD gene that prevent the body-wide translation of its protein product, dystrophin. Besides a severe muscle phenotype, cognitive impairment and neuropsychiatric symptoms are prevalent. Dystrophin protein 71 (Dp71) is the majo...
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| Publicat a: | Mol Neurobiol |
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| Autors principals: | , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Springer US
2019
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7060961/ https://ncbi.nlm.nih.gov/pubmed/31836945 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12035-019-01845-w |
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