Cargando…
Simultaneous Detection of NF1, SPRED1, LZTR1, and NF2 Gene Mutations by Targeted NGS in an Italian Cohort of Suspected NF1 Patients
Neurofibromatosis type 1 (NF1) displays overlapping phenotypes with other neurocutaneous diseases such as Legius Syndrome. Here, we present results obtained using a next generation sequencing (NGS) panel including NF1, NF2, SPRED1, SMARCB1, and LZTR1 genes on Ion Torrent. Together with NGS, the Mult...
Autores principales: | Bianchessi, Donatella, Ibba, Maria Cristina, Saletti, Veronica, Blasa, Stefania, Langella, Tiziana, Paterra, Rosina, Cagnoli, Giulia Anna, Melloni, Giulia, Scuvera, Giulietta, Natacci, Federica, Cesaretti, Claudia, Finocchiaro, Gaetano, Eoli, Marica |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7349720/ https://www.ncbi.nlm.nih.gov/pubmed/32575496 http://dx.doi.org/10.3390/genes11060671 |
Ejemplares similares
-
Risk of Optic Pathway Glioma in Neurofibromatosis Type 1: No Evidence of Genotype–Phenotype Correlations in a Large Independent Cohort
por: Melloni, Giulia, et al.
Publicado: (2019) -
126 novel mutations in Italian patients with neurofibromatosis type 1
por: Bianchessi, Donatella, et al.
Publicado: (2015) -
Characterization of 22q12 Microdeletions Causing Position Effect in Rare NF2 Patients with Complex Phenotypes
por: Tritto, Viviana, et al.
Publicado: (2022) -
Non-Coding RNA and Tumor Development in Neurofibromatosis Type 1: ANRIL Rs2151280 Is Associated with Optic Glioma Development and a Mild Phenotype in Neurofibromatosis Type 1 Patients
por: Tritto, Viviana, et al.
Publicado: (2019) -
Expanding the Noonan spectrum/RASopathy NGS panel: Benefits of adding NF1 and SPRED1
por: Witkowski, Leora, et al.
Publicado: (2020)