...NF1. The aim of this study was to analyse the lateral cephalograms of NF1 patients in comparison to individuals who were...
...NF1) is a tumor suppressor gene encoding a Ras GTPase that negatively regulates Ras signaling pathways. Mutations in NF1...
...NF1) is a rare autosomal-dominant disorder caused by inactivation of NF1 tumour suppressor gene, which associates in the...
...NF1 but have children with NF1, adults with NF1 who have children with NF1, and adults with NF1 who do not have children...
...NF1) is one of the most common genetic disorders and is caused by mutations in the NF1 gene. NF1 gene mutational analysi...
...NF1) is a complex system disorder, caused by alterations in RAS pathways. NF1 adults often suffer from chronic and sever...
...NF1 and controls during a flanker task. Behaviourally, patients with NF1 perform significantly slower than controls. Spe...
...NF1 missense variant at p.Met1149, p.Arg1276, or p.Lys1423, representing three nontruncating NF1 hotspots in the Univers...
...NF1) is a genetic disorder. Up to 50% of NF1 patients develop plexiform neurofibromas (PN). Despite revisions in diagnos...
...Nf1 gene (Nf1+/⁻) exhibited greater excitability compared with wild-type mice. To determine the mechanism giving rise to...
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