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Neurofibromatosis type 1 (NF1), caused by mutational inactivation of the NF1 tumour suppressor gene, is one of the most common dominantly inherited human disord
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Neurofibromatosis type 1 is a common inherited neurogenetic disorder affecting one in 4000 individuals worldwide. Symptoms include facial and body disfigurement
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The neurofibromatoses are autosomal-dominant genetic disorders of the nervous system that primarily affect the development and growth of neural cell tissue. The
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