Publications

Use of array CGH to detect exonic copy number variants throughout the genome in autism families detects a novel deletion in TMLHE.

Celestino-Soper PB, Shaw CA, Sanders SJ, Li J, Murtha MT, Ercan-Sencicek AG, Davis L, Thomson S, Gambin T, Chinault AC, Ou Z, German JR, Milosavljevic A, Sutcliffe JS, Cook EH, Stankiewicz P, State MW, Beaudet AL

2011
Waking up to narcolepsy.

Hauser SL, Johnston SC

2011
Waking up to narcolepsy.

Hauser SL, Johnston SC

2011
A new mode of corticothalamic transmission revealed in the Gria4(-/-) model of absence epilepsy.

Paz JT, Bryant AS, Peng K, Fenno L, Yizhar O, Frankel WN, Deisseroth K, Huguenard JR

2011
A new mode of corticothalamic transmission revealed in the Gria4(-/-) model of absence epilepsy.

Paz JT, Bryant AS, Peng K, Fenno L, Yizhar O, Frankel WN, Deisseroth K, Huguenard JR

2011

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