Add to ORKGType I neurofibromatosis (NF1) is an autosomal dominant disorder caused by mutations in the gene NF1 (Ballester et al., 1990). NF1 encodes a 260 kDa protein called neurofibromin which possesses Ras–GTPase-activating protein (Ras-GAP) activity (DeClue et al.
Neurofibromatosis type 1 (NF1) is one of the most common autosomal dominant disorders. It is caused ...
Neurofibromatosis type 1 (NF1) is one of the most common autosomal dominant disorders. It is caused ...
Neurofibromin is the product of the NF1 gene, whose alteration is responsible for the pathogenesis o...
Type I neurofibromatosis (NF1) is an autosomal dominant disorder caused by mutations in the gene NF1...
Neurofibromatosis type 1 (NF1) is a disorder caused by mutations in a single gene. These mutations r...
Neurofibromatosis type 1 (NF 1 ) is one of dm most common autosomal dominant conditions in humans (...
Neurofibromatosis type 1 (NF1) is a common familial tumour syndrome with multiple clinical features ...
* These authors contributed equally to this work. Neurofibromatosis type 1 (NF1) is one of the most ...
Neurofibromatosis type 1 (NF1) is one of the most common inherited neurological disorders with a wid...
Neurofibromatosis type-1 (NF1) is caused by constitutional mutations of the NF1 tumor-suppressor g...
Neurofibromatosis Type 1 (NF1) is one of the most com-mon genetic disorders affecting the nervous sy...
Neurofibromatosis type-1 (NF1) is caused by constitutional mutations of the NF1 tumor-suppressor g...
Neurofibromatosis type 1 (NF1) is a multisystemic disease with autosomic dominant trasmission charac...
Neurofibromatosis type 1 is a rare neurogenetic syndrome, characterized by pigmentary abnormalities,...
Neurofibromatosis type 1 (NF1) is one of the most common autosomal dominant disorders. It is caused ...
Neurofibromatosis type 1 (NF1) is one of the most common autosomal dominant disorders. It is caused ...
Neurofibromatosis type 1 (NF1) is one of the most common autosomal dominant disorders. It is caused ...
Neurofibromin is the product of the NF1 gene, whose alteration is responsible for the pathogenesis o...
Type I neurofibromatosis (NF1) is an autosomal dominant disorder caused by mutations in the gene NF1...
Neurofibromatosis type 1 (NF1) is a disorder caused by mutations in a single gene. These mutations r...
Neurofibromatosis type 1 (NF 1 ) is one of dm most common autosomal dominant conditions in humans (...
Neurofibromatosis type 1 (NF1) is a common familial tumour syndrome with multiple clinical features ...
* These authors contributed equally to this work. Neurofibromatosis type 1 (NF1) is one of the most ...
Neurofibromatosis type 1 (NF1) is one of the most common inherited neurological disorders with a wid...
Neurofibromatosis type-1 (NF1) is caused by constitutional mutations of the NF1 tumor-suppressor g...
Neurofibromatosis Type 1 (NF1) is one of the most com-mon genetic disorders affecting the nervous sy...
Neurofibromatosis type-1 (NF1) is caused by constitutional mutations of the NF1 tumor-suppressor g...
Neurofibromatosis type 1 (NF1) is a multisystemic disease with autosomic dominant trasmission charac...
Neurofibromatosis type 1 is a rare neurogenetic syndrome, characterized by pigmentary abnormalities,...
Neurofibromatosis type 1 (NF1) is one of the most common autosomal dominant disorders. It is caused ...
Neurofibromatosis type 1 (NF1) is one of the most common autosomal dominant disorders. It is caused ...
Neurofibromatosis type 1 (NF1) is one of the most common autosomal dominant disorders. It is caused ...
Neurofibromin is the product of the NF1 gene, whose alteration is responsible for the pathogenesis o...