NF1 heterozygosity fosters de novo tumorigenesis but impairs malignant transformation
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Physics and Astronomy,General Biochemistry, Genetics and Molecular Biology,General Chemistry
Link
http://www.nature.com/articles/s41467-018-07452-y.pdf
Reference67 articles.
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3. Brosseau, J. P. et al. The biology of cutaneous neurofibromas: consensus recommendations for setting research priorities. Neurology 91, S14–S20 (2018).
4. Upadhyaya, M. et al. An absence of cutaneous neurofibromas associated with a 3-bp inframe deletion in exon 17 of the NF1 gene (c.2970-2972 delAAT): evidence of a clinically significant NF1 genotype-phenotype correlation. Am. J. Hum. Genet. 80, 140–151 (2007).
5. Rojnueangnit, K. et al. High incidence of Noonan syndrome features including short stature and pulmonic stenosis in patients carrying NF1 missense mutations affecting p.Arg1809: genotype-phenotype correlation. Human. Mutat. 36, 1052–1063 (2015).
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