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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

Mendelian DisorderGenetic DisorderGenetic EpidemiologyNf1 GenePathology3-Bp Inframe DeletionNeurologyDermatologyNeuropathologyMedicineExon 17