Clinico-pathological and biomolecular findings in Italian patients with multiple cutaneous neurofibromas

BACKGROUND: Neurofibroma occurs as isolated or multiple lesions frequently associated with neurofibromatosis type 1 (NF1), a common autosomal dominant disorder affecting 1 in 3500 individuals. It is caused by mutations in the NF1 gene, which comprises 60 exons and is located on chromosome 17q11.2. N...

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Detalles Bibliográficos
Autores principales: Ponti, Giovanni, Losi, Lorena, Martorana, Davide, Priola, Manuela, Boni, Elisa, Pollio, Annamaria, Neri, Tauro Maria, Seidenari, Stefania
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3199899/
https://www.ncbi.nlm.nih.gov/pubmed/21838856
http://dx.doi.org/10.1186/1897-4287-9-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3199899/
https://www.ncbi.nlm.nih.gov/pubmed/21838856
http://dx.doi.org/10.1186/1897-4287-9-6

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