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Myogenic bladder defects in mouse models of human oculodentodigital dysplasia
To date, over 65 mutations in the gene encoding Cx43 (connexin43) have been linked to the autosomal-dominant disease ODDD (oculodentodigital dysplasia). A subset of these patients experience bladder incontinence which could be due to underlying neurogenic deterioration or aberrant myogenic regulatio...
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| Publicado no: | Biochem J |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4457304/ https://ncbi.nlm.nih.gov/pubmed/24228978 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1042/BJ20130810 |
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