Toward risk stratification and personalized therapy for neurofibromas in neurofibromatosis type 1
Author:
Affiliation:
1. Department of Neurology, Johns Hopkins University , Baltimore, MD
2. Department of Dermatology, Stanford University School of Medicine , Stanford, CA , USA
Publisher
Oxford University Press (OUP)
Subject
Dermatology
Link
https://academic.oup.com/bjd/advance-article-pdf/doi/10.1093/bjd/ljad452/54703064/ljad452.pdf
Reference6 articles.
1. Cutaneous neurofibromas: current clinical and pathologic issues;Ortonne;Neurology,2018
2. Impact of neurofibromatosis 1 on quality of life: a cross-sectional study of 176 American cases;Page;Am J Med Genet A,2006
3. ClinVar: improving access to variant interpretations and supporting evidence;Landrum;Nucleic Acids Res,2018
4. REiNS International Collaboration. Genotype–phenotype correlations in neurofibromatosis and their potential clinical use;Bettegowda;Neurology,2021
5. Identification of potential common genetic modifiers of neurofibromas: a genome wide association study in 1333 neurofibromatosis type 1 patients;Pacot;Br J Dermatol,2024
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