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Mutation spectrum of the FLCN gene responsible for BHD syndrome. Top of... | Download Scientific Diagram
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Figure 4 from A Case of Birt-Hogg-Dubé (BHD) Syndrome Harboring a Novel Folliculin (FLCN) Gene Mutation | Semantic Scholar
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A systematic review assessing the existence of pneumothorax-only variants of FLCN. Implications for lifelong surveillance of renal tumours | European Journal of Human Genetics
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Genetic screening of the FLCN gene identify six novel variants and a Danish founder mutation | Journal of Human Genetics
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Genotypic characteristics of Chinese patients with BHD syndrome and functional analysis of FLCN variants | Orphanet Journal of Rare Diseases | Full Text
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FLCN pathway. (a) FLCN is the gene associated with BHD. Normal FCLN... | Download Scientific Diagram
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A FLCN-TFE3 Feedback Loop Prevents Excessive Glycogenesis and Phagocyte Activation by Regulating Lysosome Activity - ScienceDirect
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Schemes of the FLCN/FNIP1/FNIP2 pathway. Yellow and light blue show... | Download Scientific Diagram
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