PKD mutations and evaluation of same
US8771946B2 · kind B2 · utility
0Cited by
7References
5Claims
0Family size
Assignees
Inventors
Key dates
| Filing date | Jul 24, 2007 |
| Grant date | Jul 8, 2014 |
| Priority date | — |
| Expiry date | Jun 8, 2029 |
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.