Note: You clicked on an external link, which has been disabled in order to keep your shopping session open.
FLCN is located within the Smith-Magenis syndrome region on chromosome 17. Mutations in FLCN are associated with Birt-Hogg-Dube syndrome, which is characterized by fibrofolliculomas, renal tumors, lung cysts, and pneumothorax. Alternative splicing of FLCN results in two transcript variants encoding different isoforms.
Please enter the information below and press OK to send your cart to Core Services for purchase.