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Identifying gene mutations of Chinese patients with polycystic kidney disease through targeted next‐generation sequencing technology
BACKGROUND: Polycystic kidney disease (PKD) is the most common hereditary kidney disease. The main mutational genes causing autosomal dominant polycystic kidney disease (ADPKD) are PKD1 and PKD2 as well as some rare pathogenic genes. Unilateral PKD is rare in clinics, and its association with gene m...
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| Publicat a: | Mol Genet Genomic Med |
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| Autors principals: | , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
John Wiley and Sons Inc.
2019
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6565597/ https://ncbi.nlm.nih.gov/pubmed/31056860 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.720 |
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