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PDE1A polymorphism contributes to the susceptibility of nephrolithiasis
BACKGROUND: Previous studies have confirmed a family risk of nephrolithiasis (NL), but only 15% of all cases are associated with an identified monogenic factor. In clinical practice, our group encountered a patient with NL combined with cystic kidney disease that had 3 affected family members. No kn...
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| Publicado no: | BMC Genomics |
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| Main Authors: | , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5738135/ https://ncbi.nlm.nih.gov/pubmed/29262781 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12864-017-4247-8 |
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