Associated Papers
In-silico Analysis of NF1 Missense Variants in ClinVar: Translating Variant Predictions into Variant Interpretation and Classification.
Accetturo M et al.
International Journal of Molecular Sciences, 2020
31979111 (PubMed )
Supplement: ijms-21-00721-s001.zip › ijms-614345-supplementary_files › Supplementary_Table_S3.xlsx › Suppl._Table_S3
Identification of a missense mutation causing exon skipping in a neurofibromatosis type 1 patient.
Fu Y et al.
The Journal of Dermatology, 2018
Patterns of Novel Alleles and Genotype/Phenotype Correlations Resulting from the Analysis of 108 Previously Undetected Mutations in Patients Affected by Neurofibromatosis Type I.
Bonatti F et al.
International Journal of Molecular Sciences, 2017
28961165 (PubMed )
Supplement: ijms-18-02071-s001.pdf
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