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A mouse model of urofacial syndrome with dysfunctional urination
Urofacial syndrome (UFS) is an autosomal recessive disease with severe dysfunctional urination including urinary incontinence (UI). Biallelic mutations of HPSE2 are discovered from UFS patients, suggesting that HPSE2 is a candidate disease gene. Here, we show that deletion of Hpse2 is sufficient to...
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| Publicat a: | Hum Mol Genet |
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| Autors principals: | , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Oxford University Press
2015
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4355027/ https://ncbi.nlm.nih.gov/pubmed/25510506 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddu613 |
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