Pedigree of neurofibromatosis type 1 in Libyan patients and primer design of NF1 gene

Khadija Khalifa
Background: neurofibromatosis type 1 is one of the most common genetic disorders and is caused by mutation in Nf1 gene, is characterized by is high mutation rate (about 50% of the cases are de novo). NF1 gene mutational analysis presents a considerable challenge because of its large size. This disease has been reported in several regions and cities of Libya, through the registry database in dermatology departments of Tripoli Central Hospital. The proportion of the...
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