PKD mutations and evaluation of same
US10760128B2 · kind B2 · utility
0Cited by
8References
6Claims
0Family size
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Key dates
| Filing date | May 28, 2014 |
| Grant date | Sep 1, 2020 |
| Priority date | — |
| Expiry date | May 28, 2034 |
Classification
- Technology area (CPC C)Chemistry; Metallurgy
- CPC primaryC12Q2600/158
- WIPO fieldBiotechnology
- WIPO sectorChemistry
Abstract
The present invention relates to methods of detecting novel mutations in a PKD1 and/or PKD2 gene that have been determined to be associated with autosomal dominant polycystic kidney disease (ADPKD) in order to detect or predict the occurrence of ADPKD in an individual.
Source: USPTO / EPO open patent data. Objective bibliographic and citation counts.