Analysis of the SCAI CAG repeat in a large number of families with dominant ataxia: Clinical and molecular correlations

Annals of Neurology

Volumn 37, Issue 2, 1995, Pages 176-180

  Dubourg, O ^a   Durr A ^a   Cancel, G ^a   Stevanin, G ^a   Penet, C ^a   Agid, Y ^a   Brice, A ^a   Chneiweiss, H ^b  

^a Hôpital de la Salpétrière ^*  (United States)

^b l'alimentation et l'Environnement   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CEREBELLAR ATAXIA; CHROMOSOMAL LOCALIZATION; CHROMOSOME 6P; CLINICAL FEATURE; DEGENERATIVE DISEASE; DIAGNOSIS; ETIOLOGY; FEMALE; GENE FREQUENCY; GENE MUTATION; GENETIC ANALYSIS; GENETIC LINKAGE; HUMAN; HUMAN CELL; HUNTINGTON CHOREA; MAJOR CLINICAL STUDY; MALE; NEUROTRANSMISSION; PRIORITY JOURNAL; PROGENY;

ADULT; AGE OF ONSET; CEREBELLAR ATAXIA; CHILD; CHROMOSOMES, HUMAN, PAIR 6; DNA; FEMALE; GENES, DOMINANT; HUMAN; MALE; MIDDLE AGE; MUTATION; REPETITIVE SEQUENCES, NUCLEIC ACID; SUPPORT, NON-U.S. GOV'T;

EID: 0028877774     PISSN: 03645134     EISSN: 15318249     Source Type: Journal    
DOI: 10.1002/ana.410370207     Document Type: Article

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