16p11.2 600 kb Duplications confer risk for typical and atypical Rolandic epilepsy (original) (raw)
2014, Human Molecular Genetics
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12 pages
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Rolandic epilepsy (RE) is the most common idiopathic focal childhood epilepsy. Its molecular basis is largely unknown and a complex genetic etiology is assumed in the majority of affected individuals. The present study tested whether six large recurrent copy number variants at 1q21, 15q11.