Distinct distribution of autosomal dominant spinocerebellar ataxia in the Mexican population

Movement Disorders

Volumn 22, Issue 7, 2007, Pages 1050-1053

  Alonso, Elisa ^a   Martínez Ruano, Leticia ^a   De Biase, Irene ^b   Mader, Christopher ^c   Ochoa, Adriana ^a   Yescas, Petra ^a   Gutiérrez, Roxana ^d   White, Misti ^e   Ruano, Luís ^a   Fragoso Benítez, Marcela ^f   Ashizawa, Tetsuo ^e   Bidichandani, Sanjay I ^b   Rasmussen, Astrid ^a,b  

^a NATIONAL INSTITUTE OF NEUROLOGY AND NEUROSURGERY   (Mexico)

^b UNIVERSITY OF OKLAHOMA COLLEGE OF MEDICINE   (United States)

^c UNIVERSIDAD NACIONAL AUTÓNOMA DE MÉXICO   (Mexico)

^d UNIVERSIDAD NACIONAL AUTÓNOMA DE MÉXICO   (Mexico)

^e University of Texas Medical Branch School of Medicine   (United States)

^f UNIVERSIDAD LA SALLE   (Mexico)

Author keywords

Ataxia; Autosomal dominant; Mexican population

Indexed keywords

ADENINE; ATAXIN 1; ATAXIN 3; ATAXIN 7; CYTOSINE; GUANINE; SPINOCEREBELLAR ATAXIA 10 PROTEIN; SPINOCEREBELLAR ATAXIA 12 PROTEIN; SPINOCEREBELLAR ATAXIA 17 PROTEIN; SPINOCEREBELLAR ATAXIA 2 PROTEIN; SPINOCEREBELLAR ATAXIA 6 PROTEIN; SPINOCEREBELLAR ATAXIA 8 PROTEIN; UNCLASSIFIED DRUG;

ADULT; ALLELE; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CONTROLLED STUDY; DENTATORUBROPALLIDOLUYSIAN ATROPHY; FAMILY; FEMALE; GENE MUTATION; GEOGRAPHICAL VARIATION (SPECIES); HUMAN; MAJOR CLINICAL STUDY; MALE; MEXICO; NUCLEOTIDE SEQUENCE; ONSET AGE; PREVALENCE; PRIORITY JOURNAL; SEQUENCE ANALYSIS; SPINOCEREBELLAR DEGENERATION;

CALCIUM CHANNELS; FEMALE; GENES, DOMINANT; HUMANS; MALE; MEXICO; MUTATION; NERVE TISSUE PROTEINS; NUCLEAR PROTEINS; PEDIGREE; SPINOCEREBELLAR ATAXIAS; TRINUCLEOTIDE REPEAT EXPANSION;

EID: 34347231996     PISSN: 08853185     EISSN: 15318257     Source Type: Journal    
DOI: 10.1002/mds.21470     Document Type: Article

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