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GABRB3
LE WE PMID CA
GABRB38727GABRB3

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)

Juvenile myoclonic epilepsy

KCC3

Receptor (GABA A)

Receptor (GABA)

Transporter (Chloride and potassium)

UBE3A

2010  
1
Mutations in GABAA receptor subunits associated with genetic epilepsies.
[20308251] J Physiol 588(Pt 11): 1861-9 (2010)
2010  
2
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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