Genomic structure of FLCN gene and the mutation identified in the... | Download Scientific Diagram
Mutation analysis of the FLCN gene. Sequencing of exon 12 of the FLCN... | Download Scientific Diagram
Kidney Cancer | Oncohema Key
Establishment and characterization of BHD-F59RSVT, an immortalized cell line derived from a renal cell carcinoma in a patient with Birt–Hogg–Dubé syndrome | Laboratory Investigation
PDF] Birt-Hogg-Dubé syndrome: diagnosis and management. | Semantic Scholar
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
FLCN-regulated miRNAs suppressed reparative response in cells and pulmonary lesions of Birt-Hogg-Dubé syndrome | Thorax
Frontiers | Folliculin: A Regulator of Transcription Through AMPK and mTOR Signaling Pathways
Figure 4 from A Case of Birt-Hogg-Dubé (BHD) Syndrome Harboring a Novel Folliculin (FLCN) Gene Mutation | Semantic Scholar
Frontiers | A Novel FLCN Intragenic Deletion Identified by NGS in a BHDS Family and Literature Review
Frontiers | Nutrient Signaling and Lysosome Positioning Crosstalk Through a Multifunctional Protein, Folliculin
Mutation spectrum of the FLCN gene responsible for BHD syndrome. Top of... | Download Scientific Diagram
Genetic screening of the FLCN gene identify six novel variants and a Danish founder mutation | Journal of Human Genetics
Genotypic characteristics of Chinese patients with BHD syndrome and functional analysis of FLCN variants | Orphanet Journal of Rare Diseases | Full Text
Sequence chromatogram of the FLCN gene showed a mutation in exon 6. | Download Scientific Diagram
PRISMS - Birt-Hogg-Dubé and Smith-Magenis Syndromes: Separate Disorders Linked through 17p11.2
EN Birt Hogg Dubé syndrome - YouTube
FLCN: The causative gene for Birt-Hogg-Dubé syndrome - ScienceDirect