26 October 2016 : Case report
A Case of Birt-Hogg-Dubé (BHD) Syndrome Harboring a Novel Folliculin (FLCN) Gene Mutation
Challenging differential diagnosis, Rare disease, Educational Purpose (only if useful for a systematic review or synthesis)
DOI: 10.12659/AJCR.899407
Am J Case Rep 2016; 17:788-792
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