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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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| 出版年: | Neurosci Bull |
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| 主要な著者: | , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Springer Berlin Heidelberg
2013
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| 主題: | |
| オンライン･アクセス: | 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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