Tumor suppressor genes located on the long arm of human chromosome 17 in the region 17q11.2. Mutation of these genes is thought to cause NEUROFIBROMATOSIS 1, Watson syndrome, and LEOPARD syndrome.
See also reference (FX) in Slovak
neurofibromatóza 1 neurofibromín 1
See also reference (FX) in English
Neurofibromatosis 1 Neurofibromin 1
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