BibTex format
@article{Heinzen:2010:10.1016/j.ajhg.2010.03.018,
author = {Heinzen, EL and Radtke, RA and Urban, TJ and Cavalleri, GL and Depondt, C and Need, AC and Walley, NM and Nicoletti, P and Ge, D and Catarino, CB and Duncan, JS and Kasperaviciute, D and Tate, SK and Caboclo, LO and Sander, JW and Clayton, L and Linney, KN and Shianna, KV and Gumbs, CE and Smith, J and Cronin, KD and Maia, JM and Doherty, CP and Pandolfo, M and Leppert, D and Middleton, LT and Gibson, RA and Johnson, MR and Matthews, PM and Hosford, D and Kalviainen, R and Eriksson, K and Kantanen, A-M and Dorn, T and Hansen, J and Kraemer, G and Steinhoff, BJ and Wieser, H-G and Zumsteg, D and Ortega, M and Wood, NW and Huxley-Jones, J and Mikati, M and Gallentine, WB and Husain, AM and Buckley, PG and Stallings, RL and Podgoreanu, MV and Delanty, N and Sisodiya, SM and Goldstein, DB},
doi = {10.1016/j.ajhg.2010.03.018},
journal = {AMERICAN JOURNAL OF HUMAN GENETICS},
pages = {707--718},
title = {Rare Deletions at 16p13.11 Predispose to a Diverse Spectrum of Sporadic Epilepsy Syndromes},
url = {http://dx.doi.org/10.1016/j.ajhg.2010.03.018},
volume = {86},
year = {2010}
}