Recurrence of the T666M calcium channel CACNA1A gene mutation in familial hemiplegic migraine with progressive cerebellar ataxia

American Journal of Human Genetics

Volumn 64, Issue 1, 1999, Pages 89-98

  Ducros, A ^a   Denier, C ^a   Joutel, A ^a   Vahedi, K ^b   Michel, A ^e   Darcel, F ^e   Madigand, M ^f   Guerouaou, D ^g   Tison, F ^h   Julien, J ⁱ   Hirsch, E ^j   Chedru, F ^k   Bisgard C ^l   Lucotte, G ^m   Despres P ⁿ   Billard, C ^o   Barthez, M A ^o   Ponsot, G ^d   Bousser, M G ^b   Tournier Lasserve, E ^a,c  

^a INSERM   (France)

^b Service de Neurologie

^c HÔPITAL LARIBOISIÈRE   (France)

^d HÔPITAL SAINT VINCENT DE PAUL   (France)

^e RENNES UNIVERSITY HOSPITAL   (France)

^f Hôpital de Saint Brieuc   (France)

^g LILLE UNIVERSITY HOSPITAL   (France)

^h BORDEAUX UNIVERSITY HOSPITAL   (France)

ⁱ HAUT LÉVÊQUE HOSPITAL   (France)

^j UNIVERSITY HOSPITAL OF STRASBOURG   (France)

^k CENTRE HOSPITALIER DE MEAUX   (France)

^l AARHUS UNIVERSITY HOSPITAL   (Denmark)

^m REIMS UNIVERSITY HOSPITAL   (France)

ⁿ Service de Pédiatrie   (France)

^o UNIVERSITY HOSPITAL OF TOURS   (France)

more..

Author keywords

[No Author keywords available]

Indexed keywords

CALCIUM CHANNEL;

ARTICLE; CEREBELLAR ATAXIA; CONTROLLED STUDY; DISEASE ASSOCIATION; GENE MUTATION; GENETIC LINKAGE; GENETIC POLYMORPHISM; GENETIC SCREENING; HAPLOTYPE; HUMAN; MIGRAINE; MISSENSE MUTATION; PRIORITY JOURNAL; TRINUCLEOTIDE REPEAT;

ATAXIA;

EID: 0033364409     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/302192     Document Type: Article

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