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FXTAS, SCA10, and SCA17 in American patients with movement disorders.
- Source :
-
American journal of medical genetics. Part A [Am J Med Genet A] 2005 Jul 01; Vol. 136 (1), pp. 87-9. - Publication Year :
- 2005
- Subjects :
- Adolescent
Adult
Aged
Aged, 80 and over
Ataxia genetics
Child
Child, Preschool
Female
Fragile X Mental Retardation Protein
Humans
Male
Microsatellite Repeats genetics
Middle Aged
Movement Disorders genetics
Nerve Tissue Proteins genetics
RNA-Binding Proteins genetics
Spinocerebellar Ataxias genetics
TATA-Box Binding Protein genetics
Tremor genetics
Trinucleotide Repeat Expansion genetics
United States
Ataxia pathology
Fragile X Syndrome pathology
Movement Disorders pathology
Spinocerebellar Ataxias pathology
Tremor pathology
Subjects
Details
- Language :
- English
- ISSN :
- 1552-4825
- Volume :
- 136
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- American journal of medical genetics. Part A
- Publication Type :
- Report
- Accession number :
- 15889413
- Full Text :
- https://doi.org/10.1002/ajmg.a.30761