Intention tremor, parkinsonism, and generalized brain atrophy in male carriers of fragile X

Neurology

Volumn 57, Issue 1, 2001, Pages 127-130

  Hagerman, Randi J ^a   Leehey, M ^b   Heinrichs, W ^c   Tassone, F ^a,d   Wilson, R ^c   Hills, J ^c   Grigsby, J ^b   Gage, B ^e   Hagerman, P J ^a,d  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b UNIVERSITY OF COLORADO   (United States)

^c CHILDREN S HOSPITAL   (United States)

^d UNIVERSITY OF CALIFORNIA   (United States)

^e KAISER PERMANENTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

FRAGILE X MENTAL RETARDATION PROTEIN; GENE PRODUCT; MESSENGER RNA; UNCLASSIFIED DRUG;

ADULT; AGED; ARTICLE; BRAIN ATROPHY; CLINICAL ARTICLE; DEGENERATIVE DISEASE; FRAGILE X SYNDROME; GENE MUTATION; HETEROZYGOTE; HUMAN; MALE; PARKINSONISM; PRIORITY JOURNAL; TREMOR;

EID: 0035838379     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/WNL.57.1.127     Document Type: Article

References (10)

1. Fragile X syndrome
2. Prevalence of carriers of premutation-size alleles of the FMRI gene, and implications for the population genetics of the fragile X syndrome
3. Phenotypic involvement in females with the FMR1 gene mutation
4. Genotype-phenotype relationship in female carriers of the premutation and full mutation of FMR-1
5. Clinical involvement and protein expression in individuals with the FMR1 premutation
6. Learning-disabled males with a fragile X CGG expansion in the upper premutation size range
7. Fragile X premutation is a significant risk factor for premature ovarian failure: The International Collaborative POF in Fragile X study - Preliminary data
8. Elevated levels of FMR1 mRNA in carrier males: A new mechanism of involvement in fragile X syndrome
9. Executive functioning deficits in adult males with the fragile X permutation
10. Genetic studies of the myotonic dystrophy CTG repeat