Bibliographic Details
| Title: |
A null founder variant in NPNT, encoding nephronectin, causes autosomal recessive renal agenesis |
| Authors: |
Al‐Hamed, Mohamed H., Altuwaijri, Norah, Alsahan, Nada, Ali, Wafaa, Abdulwahab, Firdous, Alzahrani, Fatema, Majrashi, Nada, Alkuraya, Fowzan S. |
| Source: |
Clinical genetics. 102(1):61-65 |
| Availability: |
http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100153643442.0x000001&indx=1&recIds=ETOCvdc_100153643442.0x000001 |
| Database: |
British Library Document Supply Centre Inside Serials & Conference Proceedings |
