Investigation of the 15q13.3 CNV as a genetic modifier for familial epilepsies with variable phenotypes
John C Mulley, Ingrid E Scheffer, Tarishi Desai, Marta A Bayly, Bronwyn E Grinton, Danya F Vears, Samuel F Berkovic, Leanne M Dibbens
Epilepsia | WILEY-BLACKWELL | Published : 2011
We thank NHMRC, SA Pathology, MS McLeod Research Fund, and Thyne Reid Charitable Trusts for support. We thank the patients and their families for participating in our research studies and Beverley Johns and Robert Schultz for technical assistance.