Neurofibromatosis Type 1: Ocular Electrophysiological and Perimetric Anomalies

INTRODUCTION: Neurofibromatosis type 1 (NF1) is a multisystemic disease caused by the mutation of Nf1 gene located on chromosome 17q11.2. The mutation determines the loss of function of the protein neurofibromin with consequent uncontrolled cellular proliferation. Patients are characterized by a wid...

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Detalles Bibliográficos
Autores principales: Nebbioso, Marcella, Moramarco, Antonietta, Lambiase, Alessandro, Giustini, Sandra, Marenco, Marco, Miraglia, Emanuele, Fino, Pasquale, Iacovino, Chiara, Alisi, Ludovico
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2020
Materias:
Original Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7585783/
https://www.ncbi.nlm.nih.gov/pubmed/33117026
http://dx.doi.org/10.2147/EB.S255184

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7585783/
https://www.ncbi.nlm.nih.gov/pubmed/33117026
http://dx.doi.org/10.2147/EB.S255184

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