When extended genetics rescues diagnosis: a patient with CANDLE-like phenotype and de novo mutation in the gene.

Ann Rheum Dis

Pediatric Rheumatology Department, Reference Centre for Autoinflammatory Diseases and Amyloidosis (CEREMAIA), Bicêtre hospital, AP-HP, university of Paris Saclay, Le Kremlin-Bicêtre, France.

Published: March 2022

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Source
http://dx.doi.org/10.1136/annrheumdis-2021-221486DOI Listing

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