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良性家族性新生儿惊厥两家系

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出处 《中华围产医学杂志》 CAS 2006年第4期278-279,共2页 Chinese Journal of Perinatal Medicine
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参考文献7

  • 1Rogawski MA.KCNQ2/KCNQ3 K+ channels and the molecular pathogenesis of epilepsy:implications for therapy.Trends Neurosci,2000,23:393-398.
  • 2Leppert M,Anderson VE,Quattlebaum T,et al.Benign familial neonatal convulsions linked to genetic markers in chromosome 20.Nature,1989,337:647-648.
  • 3Ronen GM,Rosales TM,Connolly M,et al.Seizure characteristics in chromosome 20 benign familial neonatal convulsions.Neurology,1993,43:1355-1360.
  • 4Singh NA,Charlier C,Stauffer D,et,al.A novel potassium chan nel gene,KCNQ2,is mutated in an inherited epilepsy of newborns.Natl genet,1998,18:25-29.
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  • 6Concolino D,Iembo MA,Rossi E,et al.Familial pericentric inversion of chromosone 5 in a fmilial with Benign neonatal convulsions.J Med Genet,2002,39:214-216.
  • 7Goraya JS,Virdi VS,Parmar VR.Benign familial neonatal convulsions.Indian Pediatr,2002,39:292-295.

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