학술논문
Possible precision medicine implications from genetic testing using combined detection of sequence and intragenic copy number variants in a large cohort with childhood epilepsy.
Document Type
Article
Author
Truty, Rebecca; Patil, Nila; Sankar, Raman; Sullivan, Joseph; Millichap, John; Carvill, Gemma; Entezam, Ali; Esplin, Edward D.; Fuller, Amy; Hogue, Michelle; Johnson, Britt; Khouzam, Amirah; Kobayashi, Yuya; Lewis, Rachel; Nykamp, Keith; Riethmaier, Darlene; Westbrook, Jody; Zeman, Michelle; Nussbaum, Robert L.; Aradhya, Swaroop
Source
Epilepsia Open; Sep2019, Vol. 4 Issue 3, p397-408, 12p
Subject
Language
ISSN
24709239
Abstract
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