Neurofibromatosis type Ⅰ （NF-I） is an autosomal dominant inherited disease caused by a mutated NF-I gene on chromosome 17, which produces inactive neurofibromin. Besides caf6-au-lait spots, and multiple skin neurof...Neurofibromatosis type Ⅰ （NF-I） is an autosomal dominant inherited disease caused by a mutated NF-I gene on chromosome 17, which produces inactive neurofibromin. Besides caf6-au-lait spots, and multiple skin neurofibromas,展开更多
文摘Neurofibromatosis type Ⅰ （NF-I） is an autosomal dominant inherited disease caused by a mutated NF-I gene on chromosome 17, which produces inactive neurofibromin. Besides caf6-au-lait spots, and multiple skin neurofibromas,
