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In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
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An Exome Sequencing Study to Assess the Role of Rare Genetic Variation in Pulmonary Fibrosis

Slavé Petrovski1,2, Jamie L Todd3,4, Michael T Durheim3,4

  • 11 Institute for Genomic Medicine, Columbia University Medical Center, New York, New York.

American Journal of Respiratory and Critical Care Medicine
|January 19, 2017
PubMed
Abstract

Keywords:
collapsing analysisexome sequencinggeneticsinterstitial lung diseasepulmonary fibrosis

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