Novel K+ Channel Genes in Benign Familial Neonatal Convulsions

Epilepsia ◽  
2000 ◽  
Vol 41 (8) ◽  
pp. 1066-1067 ◽  
Author(s):  
Mark Leppert
Keyword(s):  
K Channel ◽  
Neonatal Convulsions

Molecular analysis of a mutation in the S5-H5 linker of the KCNQ2 K+ channel causing neonatal convulsions

2006 ◽  
Vol 33 (S 1) ◽  
Author(s):  
G. Naros ◽  
O. Yalcin ◽  
S. Maljevic ◽  
T.V. Wuttke ◽  
A. Dervent ◽  
...  
Keyword(s):  
Molecular Analysis ◽  
K Channel ◽  
Neonatal Convulsions

A novel KCNQ2 K+channel mutation in benign neonatal convulsions and centrotemporal spikes

Neurology ◽  
2003 ◽  
Vol 61 (1) ◽  
pp. 131-134 ◽  
Author(s):  
G. Coppola ◽  
P. Castaldo ◽  
E. Miraglia del Giudice ◽  
G. Bellini ◽  
F. Galasso ◽  
...  
Keyword(s):  
K Channel ◽  
Neonatal Convulsions ◽  
Channel Mutation

Cloning of the promoters for the beta-cell ATP-sensitive K-channel subunits Kir6.2 and SUR1

Diabetes ◽  
1998 ◽  
Vol 47 (8) ◽  
pp. 1274-1280 ◽  
Author(s):  
R. Ashfield ◽  
S. J. Ashcroft
Keyword(s):  
Beta Cell ◽  
K Channel

Identification of microsatellite markers near the human genes encoding the beta-cell ATP-sensitive K+ channel and linkage studies with NIDDM in Japanese

Diabetes ◽  
1996 ◽  
Vol 45 (2) ◽  
pp. 267-269 ◽  
Author(s):  
N. Iwasaki ◽  
M. Kawamura ◽  
K. Yamagata ◽  
N. J. Cox ◽  
S. Karibe ◽  
...  
Keyword(s):  
Beta Cell ◽  
Microsatellite Markers ◽  
K Channel ◽  
Linkage Studies ◽  
Human Genes ◽  
Genes Encoding
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