Paper Details

Paper Title

Deletion of a non-canonical regulatory sequence causes loss of Scn1a expression and epileptic phenotypes in mice.

Paper Journal Title

Genome Med

Paper Citation Count

Paper Publication Year

2021

Bio Mention

1b non-coding interval, 1b region, DS, Dravet syndrome, Mice, NaV1, SCN1A, SCN1A haploinsufficiency, Scn1a, Scn1a 1b regulatory region, Scn1a promoters, co-active promoters, epilepsy, epileptic, evolutionarily conserved 1b non-coding interval, genomic regulatory elements, mice, mouse, multiple, non, non-canonical regulatory sequence, non-coding Scn1a 1b regulatory region, non-coding promoter, patients, promoters, regulatory element, risk gene, transcriptional start site, transgenic mouse line

Mesh Descriptor

Author Name	Affiliation
Len A Pennacchio	Lawrence Berkeley National Laboratory
Len A Pennacchio	University of California berkeley
Len A Pennacchio	U.S. Department of Energy Joint Genome Institute
Len A Pennacchio	Lawrence Berkeley National Laboratory
Len A Pennacchio	U.S. Department of Energy Joint Genome Institute
Len A Pennacchio	University of California berkeley
Axel Visel	Lawrence Berkeley National Laboratory
Axel Visel	University of California
Axel Visel	University of California berkeley
Axel Visel	U.S. Department of Energy Joint Genome Institute
Diane E Dickel	Lawrence Berkeley National Laboratory
Diane E Dickel	University of California berkeley
Diane E Dickel	U.S. Department of Energy Joint Genome Institute
Alex S Nord	University of California davis
Alex S Nord	University of California davis
Alex S Nord	University of California davis
Alex S Nord	University of California davis

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