An altered GABA-A receptor function in spinocerebellar ataxia type 6 and familial hemiplegic migraine type 1 associated with the CACNA1A gene mutation

BBA Clinical

Volumn 2, Issue , 2014, Pages 56-61

  Kono, Satoshi ^a   Terada, Tatsuhiro ^a   Ouchi, Yasuomi ^a   Miyajima, Hiroaki ^a  

^a HAMAMATSU UNIVERSITY SCHOOL OF MEDICINE   (Japan)

Author keywords

CACNA1A; FHM1; Flumazenil; GABA A; PET; SCA6

Indexed keywords

4 AMINOBUTYRIC ACID A RECEPTOR; FLUMAZENIL; FLUMAZENIL C 11; FLUORODEOXYGLUCOSE F 18; PEPTIDES AND PROTEINS; SPINOCEREBELLAR ATAXIA TYPE 6 PROTEIN; UNCLASSIFIED DRUG; VOLTAGE GATED CALCIUMCHANNEL ALPHA 1A;

ADULT; ARTICLE; CEREBELLAR ATAXIA; CLINICAL ARTICLE; CONTROLLED STUDY; FAMILIAL HEMIPLEGIC MIGRAINE; FEMALE; GABAERGIC SYSTEM; GENETIC ANALYSIS; GLUCOSE METABOLISM; HUMAN; MALE; MIDDLE AGED; NERVE FUNCTION; NUCLEAR MAGNETIC RESONANCE IMAGING; NUCLEOTIDE SEQUENCE; POLYMERASE CHAIN REACTION; POSITRON EMISSION TOMOGRAPHY; RECEPTOR BINDING; YOUNG ADULT;

EID: 84907979939     PISSN: 22146474     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bbacli.2014.09.005     Document Type: Article

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