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FLCN gene

Discuss publications and research concerning the FLCN gene.

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Related literature

Experience in Molecular Genetic Diagnostics of Birt-Hogg-Dubé Syndrome: Characteristics of Identified Mutations and Evolution of the Methodological Approach.
FLCN
FLCN-mutated oncocytic tumor in the thyroid defines a biologically distinct subset characterized by metabolic remodeling and canonical oncogenic signaling suppression.
FLCN
Describing the Mutational Characteristics of Myxofibrosarcoma: An AACR Project GENIE Analysis.
FLCN
First published report of the FLCN c.1222 C > T (p.Gln408Ter) variant in a Chinese family with Birt-Hogg-Dubé syndrome and literature review.
FLCN
Birt-Hogg-Dube syndrome: A case report and case study of primary spontaneous pneumothorax caused by folliculin gene mutation.
FLCN
A Novel Mutation as a Rare Cause of Pneumothorax in a Soldier.
FLCN
Molecular chaperones: Guardians of tumor suppressor stability and function.
FLCN
FLCN: The causative gene for Birt-Hogg-Dubé syndrome.
FLCN
A novel heterozygous mutation in the Birt-Hogg-Dubé Syndrome.
FLCN
Clinical and genetic characteristics of chinese patients with Birt-Hogg-Dubé syndrome.
FLCN

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