Pathogenic copy number variants and SCN1A mutations in patients with intellectual disability and childhood-onset epilepsy.
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Fry AE, et al. Among authors: owen mj.
BMC Med Genet. 2016 Apr 26;17(1):34. doi: 10.1186/s12881-016-0294-2.
BMC Med Genet. 2016.
PMID: 27113213
Free PMC article.