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2. Pathophysiology of KCNQ channels: neonatal epilepsy and progressive deafness. Jentsch TJ; Schroeder BC; Kubisch C; Friedrich T; Stein V Epilepsia; 2000 Aug; 41(8):1068-9. PubMed ID: 10961644 [No Abstract] [Full Text] [Related]
3. A KCNQ2 splice site mutation causing benign neonatal convulsions in a Scottish family. Lee WL; Biervert C; Hallmann K; Tay A; Dean JC; Steinlein OK Neuropediatrics; 2000 Feb; 31(1):9-12. PubMed ID: 10774989 [TBL] [Abstract][Full Text] [Related]
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9. Benign familial neonatal epilepsy with mutations in two potassium channel genes. Leppert M; Singh N Curr Opin Neurol; 1999 Apr; 12(2):143-7. PubMed ID: 10226745 [TBL] [Abstract][Full Text] [Related]
10. Complete loss of the cytoplasmic carboxyl terminus of the KCNQ2 potassium channel: a novel mutation in a large Czech pedigree with benign neonatal convulsions or other epileptic phenotypes. Pereira S; Roll P; Krizova J; Genton P; Brazdil M; Kuba R; Cau P; Rektor I; Szepetowski P Epilepsia; 2004 Apr; 45(4):384-90. PubMed ID: 15030501 [TBL] [Abstract][Full Text] [Related]
11. [A novel mutation of KCNQ2 gene in a Chinese family with benign familial neonatal convulsions]. Li HY; Tang BS; Zhang AM; Cao QH; Meng GL; Jiang H; Shen L Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Dec; 20(6):482-5. PubMed ID: 14669214 [TBL] [Abstract][Full Text] [Related]
12. A de novo KCNQ2 mutation detected in non-familial benign neonatal convulsions. Ishii A; Fukuma G; Uehara A; Miyajima T; Makita Y; Hamachi A; Yasukochi M; Inoue T; Yasumoto S; Okada M; Kaneko S; Mitsudome A; Hirose S Brain Dev; 2009 Jan; 31(1):27-33. PubMed ID: 18640800 [TBL] [Abstract][Full Text] [Related]
13. A novel mutation in KCNQ2 gene causes benign familial neonatal convulsions in a Chinese family. Tang B; Li H; Xia K; Jiang H; Pan Q; Shen L; Long Z; Zhao G; Cai F J Neurol Sci; 2004 Jun; 221(1-2):31-4. PubMed ID: 15178210 [TBL] [Abstract][Full Text] [Related]
15. A novel missense mutation (N258S) in the KCNQ2 gene in a Turkish family afflicted with benign familial neonatal convulsions (BFNC). Yalçin O; Cağlayan SH; Saltik S; Cokar O; Ağan K; Dervent A; Steinlein OK Turk J Pediatr; 2007; 49(4):385-9. PubMed ID: 18246739 [TBL] [Abstract][Full Text] [Related]
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17. Study of the voltage-gated sodium channel beta 1 subunit gene (SCN1B) in the benign familial infantile convulsions syndrome (BFIC). Moulard B; Buresi C; Malafosse A Hum Mutat; 2000; 16(2):139-42. PubMed ID: 10923035 [TBL] [Abstract][Full Text] [Related]
18. De novo KCNQ2 mutations in patients with benign neonatal seizures. Claes LR; Ceulemans B; Audenaert D; Deprez L; Jansen A; Hasaerts D; Weckx S; Claeys KG; Del-Favero J; Van Broeckhoven C; De Jonghe P Neurology; 2004 Dec; 63(11):2155-8. PubMed ID: 15596769 [TBL] [Abstract][Full Text] [Related]
19. Structural and mutational analysis of KCNQ2, the major gene locus for benign familial neonatal convulsions. Biervert C; Steinlein OK Hum Genet; 1999 Mar; 104(3):234-40. PubMed ID: 10323247 [TBL] [Abstract][Full Text] [Related]
20. A potassium channel mutation in neonatal human epilepsy. Biervert C; Schroeder BC; Kubisch C; Berkovic SF; Propping P; Jentsch TJ; Steinlein OK Science; 1998 Jan; 279(5349):403-6. PubMed ID: 9430594 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]