Benign adult familial myoclonus epilepsy (BAFME): an autosomal dominant form not linked to the dentatorubral pallidoluysian atrophy (DRPLA) gene.

Author:

Kuwano A,Takakubo F,Morimoto Y,Uyama E,Uchino M,Ando M,Yasuda T,Terao A,Hayama T,Kobayashi R,Kondo I

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference8 articles.

1. Benign adult familial mvoclonus epilepsy (BAFME);Yasuda, T.;KazvasakiMed_],1991

2. Anticipation in hereditary dentatorubral-pallidoluysian atrophy;Sano, A.; Yamauchi, N.; Kakimoto, Y.;Hum Geniet,1994

3. Unstable expansion of CAG repeat in hereditary dentatorubral-pallidoluysian atrophy (DRPLA);true;Natutre Genet,1994

4. Structure and expression of the gene responsible for the triplet repeat disorder, dentatorubral and pallidoluysian atrophy (DRPLA);Nagafuchi, S.; Yanagisawa, H.; Osaki, E.;Nature Genet,1994

5. Localization of the gene encoding the GABA(A) receptor beta-3 subunit to the Angelman/Prader-Willi region of chromosome;Wastff, J.; Knoll, J.H.M.; Fleming, J.;15. Am 7 Hunm Genet,1991

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