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A genome scan in affected sib-pairs with familial vesicoureteral reflux identifies a locus on chromosome 5
The basis for vesicoureteral reflux (VUR) is considered to be primarily genetic, with a 30–50% incidence of VUR in first-degree relatives of patients. The search for the causative gene or genes has been elusive, likely because of VUR being genetically heterogeneous with complex inheritance patterns....
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| Main Authors: | , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Nature Publishing Group
2010
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2987194/ https://ncbi.nlm.nih.gov/pubmed/19690587 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2009.142 |
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