Splice-site mutation causing partial retention of intron in the FLCN gene in Birt-Hogg-Dubé syndrome: a case report | BMC Medical Genomics | Full Text
Frontiers | Nutrient Signaling and Lysosome Positioning Crosstalk Through a Multifunctional Protein, Folliculin
FLCN-regulated miRNAs suppressed reparative response in cells and pulmonary lesions of Birt-Hogg-Dubé syndrome | Thorax
Genotypic characteristics of Chinese patients with BHD syndrome and functional analysis of FLCN variants | Orphanet Journal of Rare Diseases | Full Text
FLCN: The causative gene for Birt-Hogg-Dubé syndrome - ScienceDirect
Late Onset of Skin Manifestations in Birt-Hogg-Dubé Syndrome with FLCN Mutation p.W260X | HTML | Acta Dermato-Venereologica
Sequence chromatogram of the FLCN gene showed a mutation in exon 6. | Download Scientific Diagram
JCI - Folliculin impairs breast tumor growth by repressing TFE3-dependent induction of the Warburg effect and angiogenesis
Mutation analysis of the FLCN gene. Sequencing of exon 12 of the FLCN... | Download Scientific Diagram
The genetics of BHD – Birt-Hogg-Dubé Syndrome
Frontiers | Folliculin: A Regulator of Transcription Through AMPK and mTOR Signaling Pathways
PRISMS - Birt-Hogg-Dubé and Smith-Magenis Syndromes: Separate Disorders Linked through 17p11.2
Genotypic characteristics of Chinese patients with BHD syndrome and functional analysis of FLCN variants | Orphanet Journal of Rare Diseases | Full Text
Differential mTORC1 pathways in BHD | Nature Reviews Urology
FLCN: The causative gene for Birt-Hogg-Dubé syndrome - ScienceDirect
EN Birt Hogg Dubé syndrome - YouTube
Kidney Cancer | Oncohema Key
Mutation spectrum of the FLCN gene responsible for BHD syndrome. Top of... | Download Scientific Diagram
Novel mutations in the folliculin gene associated with spontaneous pneumothorax | European Respiratory Society
Figure 4 from A Case of Birt-Hogg-Dubé (BHD) Syndrome Harboring a Novel Folliculin (FLCN) Gene Mutation | Semantic Scholar
Genetic screening of the FLCN gene identify six novel variants and a Danish founder mutation | Journal of Human Genetics
Identification of a novel frameshift mutation of the FLCN gene in the... | Download Scientific Diagram
Brit-Hogg-Dube syndrome. (A) Folliculin (FLCN) gene analysis showing a... | Download Scientific Diagram
Schemes of the FLCN/FNIP1/FNIP2 pathway. Yellow and light blue show... | Download Scientific Diagram
