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Volumn 7, Issue 2, 2001, Pages 136-145

Sodium channels and neurological disease: Insights from Scn8a mutations in the mouse

Author keywords

Dystonia; Epilepsy; Mouse mutant; Paralysis; Sodium channel

Indexed keywords

SODIUM CHANNEL;

EID: 0035076298     PISSN: 10738584     EISSN: None     Source Type: Journal    
DOI: 10.1177/107385840100700208     Document Type: Review
Times cited : (57)

References (45)
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  • 12
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    • Phenotypes of patients with "simple" mendelian disorders are complex traits: Thresholds, modifiers and systems dynamics
    • (2000) Am J Hum Genet , vol.67 , pp. 1729-1735
    • Dipple, K.M.1    McCabe, E.R.B.2
  • 14
    • 0014980365 scopus 로고
    • Electrophysiological studies of neuromuscular transmission in hereditary "motor endplate disease" of the mouse
    • (1971) J Physiol , vol.212 , pp. 535-548
    • Duchen, L.W.1    Stefani, E.2
  • 16
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    • Nerve transplantation shows that motor end-plate disease is not a primary Schwann cell defect
    • (1987) Exp Neurol , vol.97 , pp. 135-142
    • Füchtbauer, E.M.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.