메뉴 건너뛰기




Volumn 84, Issue 3, 2001, Pages 277-280

Ion channels and neurology

Author keywords

[No Author keywords available]

Indexed keywords

ION CHANNEL;

EID: 0035081337     PISSN: 00039888     EISSN: 14682044     Source Type: Journal    
DOI: 10.1136/adc.84.3.277     Document Type: Review
Times cited : (5)

References (24)
  • 2
    • 35649001607 scopus 로고
    • A quantitative description of membrane current and its application to conduction and excitation in nerve
    • (1952) J Physiol , vol.117 , pp. 500-544
    • Hodgkin, A.L.1    Huxley, A.F.2
  • 4
    • 0028980028 scopus 로고
    • A missense mutation in the neuronal nicotinic acetylcholine receptor α4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy
    • (1995) Nat Genet , vol.11 , pp. 201-203
    • Steinlein, O.1    Mulley, J.C.2    Propping, P.3
  • 5
    • 0030602149 scopus 로고    scopus 로고
    • An amino acid exchange in the second transmembrane segment of a neuronal nicotinic receptor cause partial epilepsy by altering its desensitization kinetics
    • (1996) FEBS Lett , vol.398 , pp. 91-96
    • Weiland, S.1    Witzemann, V.2    Villaroel, A.3
  • 8
    • 0032483972 scopus 로고    scopus 로고
    • KCNQ and KCNQ3 potassium channel subunits: Molecular correlates of the M-channel
    • (1998) Science , vol.282 , pp. 1890-1893
    • Wang, H.S.1    Pan, Z.2    Shi, W.3
  • 9
    • 0030943313 scopus 로고    scopus 로고
    • Generalised epilepsy with febrile seizures plus. A genetic disorder with heterogenous clinical phenotypes
    • (1997) Brain , vol.120 , pp. 479-490
    • Scheffer, I.E.1    Berkovic, S.F.2
  • 16
    • 0032895470 scopus 로고    scopus 로고
    • A novel mutation in the human voltage gated potassium channel gene (Kv1.1) associates with episodic ataxia and sometimes with partial epilepsy
    • (1999) Brain , vol.122 , pp. 817-825
    • Zuberi, S.M.1    Eunson, L.H.2    Spauschus, A.3
  • 17
    • 0033797135 scopus 로고    scopus 로고
    • Clinical, genetic and expression studies of mutations in the human voltage-gated potassium channel KCNA1 reveal new phenotypic variability
    • (2000) Ann Neurol , vol.48 , pp. 647-656
    • Eunson, L.H.1    Rea, R.2    Zuberi, S.M.3
  • 18
    • 0027330927 scopus 로고
    • Mutations in the α1A subunit of the inhibitory glycine receptor cause the dominant neurological disorder hyperekplexia
    • (1993) Nat Genet , vol.5 , pp. 351-358
    • Shiang, R.1    Ryan, S.G.2    Zhu, Y.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.