Papers: 10.1371/journal.pone.0076360

https://doi.org/10.1371/journal.pone.0076360

Targeted Exome Sequencing Integrated with Clinicopathological Information Reveals Novel and Rare Mutations in Atypical, Suspected and Unknown Cases of Alport Syndrome or Proteinuria

Cited by: 59
Author(s): Rajshekhar Chatterjee, Mary Hoffman, Paul Cliften, Surya V. Seshan, Helen Liapis, Sanjay Jain
Published: almost 13 years ago

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