Mutation of GABRA1 in an autosomal dominant form of juvenile myoclonic epilepsy

By P. Cossette, Lidong Liu, K. Brisebois, Haiheng Dong, A. Lortie, M. Vanasse, J. Saint‐Hilaire, L. Carmant, A. Verner, Wei-yang Lu and 2 more. Nature Genetics, 2002

628 citations recorded by the source corpus.

Subfields: Cellular and Molecular Neuroscience, Molecular Biology, Psychiatry and Mental health

View Paper: https://www.semanticscholar.org/paper/43cfe2c984b4aae192d84179c8a470918bc19306

Citations in the corpus

• The neurobiology of antiepileptic drugs (2004, neutral): “fcgi?db=gene&cmd=Retrieve&dopt=Graphics&list_uids=2554">GABRA1 ) that markedly reduces the function of heteromeric GABA receptors containing the subunit has been associated with autosomal dominant JUVENILE MYOCLONIC EPILEPSY in one famil”