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Infancy onset hereditary spastic paraplegia associated with a novel atlastin mutation.
- Source :
-
Neurology [Neurology] 2003 Aug 26; Vol. 61 (4), pp. 580-1. - Publication Year :
- 2003
- Subjects :
- Adolescent
Adult
Age of Onset
Amino Acid Substitution
Child
Child, Preschool
Exons genetics
Female
GTP-Binding Proteins
Gait Disorders, Neurologic genetics
Humans
Infant
Lod Score
Male
Membrane Proteins
Pedigree
Spastic Paraplegia, Hereditary diagnosis
Spastic Paraplegia, Hereditary epidemiology
GTP Phosphohydrolases genetics
Mutation, Missense
Point Mutation
Spastic Paraplegia, Hereditary genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1526-632X
- Volume :
- 61
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- Neurology
- Publication Type :
- Academic Journal
- Accession number :
- 12939451
- Full Text :
- https://doi.org/10.1212/01.wnl.0000078189.73611.df