04
Aug
NF1 microdeletions and mutations gene location chromosome 17q11.2
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Neurofibromatosis type 1 (NF1) is a hereditary syndrome. The main manifestations of this condition include café-au-lait spots, Lisch nodules and neurofibromas. It occurs in 1 to every 2000-3000 people. In most patients NF1 is caused by mutations of the NF1 gene, located at 17q11.2. However, 5-11% of patients have deletions... Read More