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Elucidating the impact of neurofibromatosis-1 germline mutations on neurofibromin function and dopamine-based learning
Neurofibromatosis type 1 (NF1) is a common autosomal dominant neurologic condition characterized by significant clinical heterogeneity, ranging from malignant cancers to cognitive deficits. Recent studies have begun to reveal rare genotype–phenotype correlations, suggesting that the specific germlin...
Tallennettuna:
| Julkaisussa: | Hum Mol Genet |
|---|---|
| Päätekijät: | , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Oxford University Press
2015
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4553714/ https://ncbi.nlm.nih.gov/pubmed/25788518 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddv103 |
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