...NF1 mouse models with reversible NF1 expression. In the first model, the human NF1 -/- Schwann cells named ipNF95.11b C/...
...NF1), and (2) whether demographic and NF1-specific factors moderated the associations. Method: We analyzed integrated cr...
...NF1) splice-site mutation c.61-2A>G (rs1131691100) is a rare, pathogenic, autosomal dominant variant that disrupts NF1 t...
...NF1 that could improve the quality of life of affected individuals.
...NF1 early helps pediatric dentists guide timely referrals and coordinated care. Even mild oral findings can impair child...
...NF1 gene, leading to constitutive RAS/MAPK pathway activation, and recurrent "MIR143-NOTCH" gene fusions disrupting Notc...
...NF1). MRI is an important preoperative diagnostic modality. Complete surgical excision remains the treatment of choice a...
...NF1 (c.2643G>A, p.Met881Ile). Subsequent testing with an expanded panel identified a pathogenic variant in MUTYH (c.1187...
...NF1. Individual I had concomitant arachnoid and odontogenic cysts in parallel with a novel heterozygous germline NF1 pat...
...NF1) and dural meningocele, successfully managed via a single-stage posterior approach-a well-established technique adap...
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