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Dravet s syndrome
LE WE PMID CA
Dravet s syndrome8721Dravet Syndrom

Action potential

Angelman s syndrome

Autosomal dominant epilepsy with febrile seizures plus

Autosomal dominant Juvenile Myoclonic Epilepsy

Childhood absence epilepsy

CLCN2 ClC2

Dravet s syndrome

Epilepsy (BASKET)

Epilepsy (Generalized epilepsy with febrile seizures plus)

Febrile convulsions

GABRA1

GABRA4

GABRA5

GABRA6

GABRB3

GABRD

GABRE

GABRG2

GABRG3

GABRP

Heart (Coronary heart disease Main stenosis)

Ion channel (Chloride)

Ion channel (Sodium)

Juvenile myoclonic epilepsy

KCC3

NaV1 1

Receptor (GABA A)

Receptor (GABA)

SCN1A

SCN2A

SCN3A

SCN8A

SCN9A

Transporter (Chloride and potassium)

UBE3A

2010  
1
Sodium channel gene family: epilepsy mutations, gene interactions and modifier effects.
[20351042] J Physiol 588(Pt 11): 1841-8 (2010)
2010  
2
Mutations in GABAA receptor subunits associated with genetic epilepsies.
[20308251] J Physiol 588(Pt 11): 1861-9 (2010)
2010  
3
2010  
4
Mutations affecting GABAergic signaling in seizures and epilepsy.
[20352446] Pflugers Arch 460(2): 505-23 (2010)

Downloaded from http://www.kidney.de - The Database of Free Medical Reviews - The Metatextbook of Medicine - Ossip Groth

All Medline data shown were primarily retrieved from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.


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