Targeted exome sequencing integrated with clinicopathological information reveals novel and rare mutations in atypical, suspected and unknown cases of Alport syndrome or proteinuria

Authors

Rajshekhar Chatterjee, Washington University School of Medicine in St. Louis
Mary Hoffman, Washington University School of Medicine in St. Louis
Paul Cliften, Washington University School of Medicine in St. Louis
Surya Seshan, Cornell University
Helen Liapis, Washington University School of Medicine in St. Louis
Sanjay Jain, Washington University School of Medicine in St. Louis

Journal

PLoS One

Publication Date

2013

Volume

8

Issue

10

Inclusive Pages

e76360

Document Type

Open Access Publication

DOI

10.1371/journal.pone.0076360

Rights and Permissions

Chatterjee R, Hoffman M, Cliften P, Seshan S, Liapis H, et al. (2013) Targeted Exome Sequencing Integrated with Clinicopathological Information Reveals Novel and Rare Mutations in Atypical, Suspected and Unknown Cases of Alport Syndrome or Proteinuria. PLoS ONE 8(10): e76360. doi:10.1371/journal.pone.0076360

Recommended Citation

Chatterjee, Rajshekhar; Hoffman, Mary; Cliften, Paul; Seshan, Surya; Liapis, Helen; and Jain, Sanjay, "Targeted exome sequencing integrated with clinicopathological information reveals novel and rare mutations in atypical, suspected and unknown cases of Alport syndrome or proteinuria." PLoS One. 8, 10. e76360. (2013).
https://digitalcommons.wustl.edu/open_access_pubs/1723