Art

J-GLOBAL ID：200902120182567229   Reference number：02A0781711

Genetics of epilepsy: Current status and perspectives.

てんかんの遺伝学 現状と展望

Author (5)： KANEKO S (Hirosaki Univ., Hirosaki, JPN) ,  OKADA M (Hirosaki Univ., Hirosaki, JPN) ,  IWASA H (Hirosaki Univ., Hirosaki, JPN) ,  YAMAKAWA K (RIKEN Brain Sci., Inst., Saitama, JPN) ,  HIROSE S (Fukuoka Univ., Fukuoka, JPN)
Material： Neuroscience Research  (神経科学)
Volume： 44  Issue： 1  Page： 11-30  Publication year： Sep. 2002 
JST Material Number： D0210C  ISSN： 0168-0102  Document type： Article
Article type： 文献レビュー  Country of issue： Netherlands (NLD)  Language： ENGLISH (EN)

Thesaurus term： *Epilepsy ,...

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JST classification (2)： Central nervous system  (EJ12030F) ,  Nervous system diseases  (GN03000O)

Reference (167)：

• Nomenclature Working Group. Recommendations for a nomenclature system for human gene mutations. Hum. Mutat. 1998, 11, 1-3
• ARMSTRONG, L. C. Metaxin is a component of a preprotein import complex in the outer membrane of the mammalian mitochondrion. J. Biol. Chem. 1997, 272, 6510-6518
• BARAISTER, M. The Genetics of Neurological Disorders. 1990, 96-113
• BAULAC, S. First evidence of GABA receptor dysfunction in epilepsy : a mutation in the γ2-subunit gene. Nat. Genet. 2001, 28, 46-48
• BECK, M. Neuraminidase deficiency presenting as non-immune hydrops fetalis. Eur. J. Pediatr. 1984, 143, 135-139

Terms in the title (4)： てんかん ,  遺伝学 ,  現状 ,  展望