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Ultra-Rare Genetic Variation in Relapsing Polychondritis: A Whole-Exome Sequencing Study

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By Ferrada MA, Sikora KA, Kastner DL, Merkel PA
| ncbi.nlm.nih.gov
This is a preprint. It has not yet been peer reviewed by a journal. The National Library of Medicine is running a pilot to include preprints that result from research funded by NIH in PMC and PubMed. Display options Abstract Objective: Relapsing polychondritis (RP) is a systemic inflammatory disease of unknown etiology. The study objective was to examine the contribution of rare genetic variations in RP.
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