Examination of the genetic factors underlying the cognitive variability associated with neurofibromatosis type 1
Author:
Funder
Stichting Neurofibromatose
Publisher
Elsevier BV
Subject
Genetics (clinical)
Link
http://www.nature.com/articles/s41436-020-0752-2.pdf
Reference45 articles.
Cited by 21 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Genotype–phenotype correlations of neurofibromatosis type 1: a cross-sectional study from a large Chinese cohort;Journal of Neurology;2023-12-14
2. SLC6A1 variant pathogenicity, molecular function and phenotype: a genetic and clinical analysis;Brain;2023-08-30
3. The contribution of morbidity and unemployment for the reduced labor market participation of individuals with neurofibromatosis 1 in Finland;European Journal of Human Genetics;2023-07-18
4. Visual–spatial and visuomotor functioning in adults with neurofibromatosis type 1;Journal of Intellectual Disability Research;2023-01-09
5. Cerebellum-dependent associative learning is not impaired in a mouse model of neurofibromatosis type 1;Scientific Reports;2022-11-09
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