Targeted Exome Sequencing Integrated with Clinicopathological Information Reveals Novel and Rare Mutations in Atypical, Suspected and Unknown Cases of Alport Syndrome or Proteinuria
Abstract
- Publication:
-
PLoS ONE
- Pub Date:
- October 2013
- DOI:
- 10.1371/journal.pone.0076360
- Bibcode:
- 2013PLoSO...876360C