Clinical features and ATTCT repeat expansion in spinocerebellar ataxia type 10

Archives of Neurology

Volumn 59, Issue 8, 2002, Pages 1285-1290

  Grewal, Raji P ^a   Achari, Madhureeta ^e   Matsuura, Tohru ^b   Durazo, Alberto ^e   Tayag, Emilio ^c   Zu, Lan ^d   Pulst, Stefan M ^d   Ashizawa, Tetsuo ^b  

^a SETON HALL UNIVERSITY   (United States)

^b BAYLOR COLLEGE OF MEDICINE   (United States)

^c UNIVERSITY OF SOUTHERN CALIFORNIA   (United States)

^d UNIVERSITY OF CALIFORNIA   (United States)

^e NONE

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CEREBELLUM ATROPHY; CLINICAL ARTICLE; CLINICAL FEATURE; COMPUTER ASSISTED TOMOGRAPHY; CORRELATION ANALYSIS; ELECTROENCEPHALOGRAM; EPILEPTIC DISCHARGE; FEMALE; GENOTYPE; HUMAN; MALE; NUCLEOTIDE REPEAT; PATHOGENESIS; PEDIGREE; PHENOTYPE; PRIORITY JOURNAL; SCHOOL CHILD; SEIZURE; SPINOCEREBELLAR DEGENERATION;

ADULT; CHILD; EPILEPSY, COMPLEX PARTIAL; FAMILY HEALTH; FEMALE; GENOTYPE; HUMANS; MAGNETIC RESONANCE IMAGING; MALE; MIDDLE AGED; PEDIGREE; PHENOTYPE; REPETITIVE SEQUENCES, NUCLEIC ACID; SPINOCEREBELLAR ATAXIAS;

EID: 0036340277     PISSN: 00039942     EISSN: None     Source Type: Journal    
DOI: 10.1001/archneur.59.8.1285     Document Type: Article

References (16)

1. Hereditary ataxias
2. Clinical features and classification of the inherited ataxias
3. Autosomal dominant cerebellar phenotypes: The genotype has settled the issue
4. Genetic testing in spinocerebellar ataxias: Defining a clinical role
5. Mapping of spinocerebellar ataxia 13 to chromosome 19q13.3-q13.4 in a family with autosomal dominant cerebellar ataxia and mental retardation
6. A novel locus for dominant cerebellar ataxia (SCA14) maps to a 10.2-cM interval flanked by D19S206and D19S605on chromosome 19q13.40-qter
7. A novel autosomal dominant spinocerebellar ataxia (SCA16) linked to chromosome 8q22.1-24.1
8. SCA17, a novel autosomal dominant cerebellar ataxia caused by an expanded polyglutamine in TATA-binding protein
9. Clinical and genetic analysis of a distinct autosomal dominant spinocerebellar ataxia
10. Mapping of a new autosomal dominant spinocerebellar ataxia to chromosome 22
11. Mapping of the gene for a novel spinocerebellar ataxia with pure cerebellar signs and epilepsy
12. Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10
13. Calcified neurocysticercotic lesions and postsurgery seizure control in temportal lobe epilepsy
14. Hemifacial seizures and cerebellar gangliomana: An epilepsy syndrome of infancy with seizures of cerebellar origin
15. Clinical and genetic analysis of four Mexican families with spinocerebellar ataxia type 10
16. Somatic mosaicism, germline expansions, germline reversions and intergenerational reductions in myotonic dystrophy males: Small pool PCR analyses