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Cerebral vasculopathy in a Chinese family with neurofibromatosis type I mutation
Neurofibromatosis type I (NF1) is a hereditary, autosomal dominant, neurocutaneous syndrome that is attributed to NF1 gene mutation. NF1 has been associated with scoliosis, macrocephaly, pseudoarthrosis, short stature, mental retardation, and malignancies. NF1-associated vasculopathy is an uncommon...
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| Publicat a: | Neurosci Bull |
|---|---|
| Autors principals: | , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Springer Berlin Heidelberg
2013
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5562553/ https://ncbi.nlm.nih.gov/pubmed/24218100 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12264-013-1388-x |
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