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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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| Publicado no: | Eye Brain |
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| Main Authors: | , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Dove
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7585783/ https://ncbi.nlm.nih.gov/pubmed/33117026 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/EB.S255184 |
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