TY  - GEN
AU  - Reid,E
AU  - Dearlove,A M
AU  - Osborn,O
AU  - Rogers,M T
AU  - Rubinsztein,D C
TI  - A locus for autosomal dominant "pure" hereditary spastic paraplegia maps to chromosome 19q13
SN  - 0002-9297
PY  - 2000///0330
KW  - Adolescent
KW  - Adult
KW  - Age of Onset
KW  - Child
KW  - Child, Preschool
KW  - Chromosome Mapping
KW  - Chromosomes, Human, Pair 19
KW  - genetics
KW  - Female
KW  - Genes, Dominant
KW  - Genetic Heterogeneity
KW  - Haplotypes
KW  - Humans
KW  - Lod Score
KW  - Male
KW  - Microsatellite Repeats
KW  - Paraplegia
KW  - epidemiology
KW  - Pedigree
KW  - Penetrance
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1086/302783
ER  -