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Resting state functional MRI reveals abnormal network connectivity in neurofibromatosis 1
Neurofibromatosis type I (NF1) is a genetic disorder caused by mutations in the neurofibromin 1 gene at locus 17q11.2. Individuals with NF1 have an increased incidence of learning disabilities, attention deficits, and autism spectrum disorders. As a single‐gene disorder, NF1 represents a valuable mo...
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發表在: | Hum Brain Mapp |
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Main Authors: | , , , , , , , , |
格式: | Artigo |
語言: | Inglês |
出版: |
John Wiley and Sons Inc.
2015
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主題: | |
在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4619152/ https://ncbi.nlm.nih.gov/pubmed/26304096 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/hbm.22937 |
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