The Sacred Disease: The Puzzling Genetics of Epileptic Disorders

Neuron

Volumn 80, Issue 1, 2013, Pages 9-11

  Novarino, Gaia ^a   Baek, SeungTae ^a   Gleeson, Joseph G ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

4 AMINOBUTYRIC ACID A RECEPTOR BETA3; MAMMALIAN TARGET OF RAPAMYCIN; UBIQUITIN PROTEIN LIGASE NEDD4;

AUTISM; AUTOSOMAL RECESSIVE INHERITANCE; DE NOVO MUTATION; EPILEPSY; EPILEPTIC ENCEPHALOPATHY; EXOME; GABRB3 GENE; GENE MUTATION; GENETIC RISK; HAPPY PUPPET SYNDROME; HUMAN; INFANTILE SPASM; INTELLECTUAL IMPAIRMENT; LENNOX GASTAUT SYNDROME; LOSS OF FUNCTION MUTATION; PRIORITY JOURNAL; SEQUENCE ANALYSIS; SHORT SURVEY; SOMATIC MUTATION; WHOLE EXOME SEQUENCING;

FEMALE; HUMANS; INTELLECTUAL DISABILITY; MALE; MUTATION; SPASMS, INFANTILE;

EID: 84884752719     PISSN: 08966273     EISSN: 10974199     Source Type: Journal    
DOI: 10.1016/j.neuron.2013.09.019     Document Type: Short Survey

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