Showing results 1 to 3 of 3
Title | Author(s) | Issue Date | |
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Two-stage genome-wide association study identifies variants in CAMSAP1L1 as susceptibility loci for epilepsy in Chinese Journal:Human Molecular Genetics | 2012 | ||
2012 | |||
A 1.36-megabase deletion in chromosome 18q21.32 including GRP in a patient with epilepsy, borderline intellectual disability, and multiple cerebral cavernous malformations Book:Biochemistry and Molecular Biology: The Complexity of Human Traits and Diseases | 2015 |