Autosomal dominant cerebellar ataxia type I in Martinique (French West Indies): Genetic analysis of three unrelated SCA2 families

Human Genetics

Volumn 97, Issue 5, 1996, Pages 671-676

  Lezin, Agnès ^a   Cancel, Géraldine ^b   Stevanin, Giovanni ^b   Smadja, Didier ^c   Vernant, Jean Claude ^c   Dürr, Alexandra ^b   Martial, Jenny ^a   Buisson, Georges Gabriel ^c   Bellance, Rémy ^c   Chneiweiss, Hervé ^d   Agid, Yves ^b   Brice, Alexis ^b  

^a Lab de Biologie Moléculaire   (Martinique)

^b PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

^c CENTRE HOSPITALIER UNIVERSITAIRE DE FORT DE FRANCE   (France)

^d PSL Research University   (France)

Author keywords

[No Author keywords available]

Indexed keywords

TRINUCLEOTIDE;

ADOLESCENT; ADULT; AGED; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CEREBELLAR ATAXIA; CHILD; CHROMOSOME 12Q; CLINICAL ARTICLE; CONTROLLED STUDY; FEMALE; FOUNDER EFFECT; GENE LOCUS; GENETIC ANALYSIS; GENETIC LINKAGE; GENETIC RECOMBINATION; HAPLOTYPE; HUMAN; HUMAN CELL; INFANT; MALE; MARKER GENE; MARTINIQUE; PRIORITY JOURNAL;

ATAXIA;

EID: 13344268998     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/BF02281881     Document Type: Article

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