SomaticNF1 mutation spectra in a family with neurofibromatosis type 1: Toward a theory of genetic modifiers
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Reference24 articles.
1. Aberrant regulation of ras proteins in malignant tumour cells from type 1 neurofibromatosis patients
2. Benign neurofibromas in type 1 neurofibromatosis (NF1) show somatic deletions of the NF1 gene
3. Clonal Origin of Tumor Cells in a Plexiform Neurofibroma with LOH in NF1 Intron 38 and in Dermal Neurofibromas without LOH of the NF1 Gene
4. Abnormal regulation of mammalian p21ras contributes to malignant tumor growth in von Recklinghausen (type 1) neurofibromatosis
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3. Novel Mutation C.7348C>T in NF1 Gene Identified by Whole-Exome Sequencing in Patient with Overlapping Clinical Symptoms of Neurofibromatosis Type 1 and Bannayan–Riley–Ruvalcaba Syndrome;Cytology and Genetics;2020-07
4. Clinical and molecular characteristics of thirty NF1 variants in Chinese patients with neurofibromatosis type 1;Molecular Biology Reports;2019-06-14
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