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Autosomal dominant spastic paraplegia: refined SPG8 locus and additional genetic heterogeneity.

Reid, E

Autosomal dominant spastic paraplegia: refined SPG8 locus and additional genetic heterogeneity. [electronic resource] - Neurology Nov 1999 - 1844-9 p. digital

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

ISSN: 0028-3878

Standard No.: 10.1212/wnl.53.8.1844 doi

Subjects--Topical Terms:
Adult
Chromosome Mapping
Chromosomes, Human, Pair 8
Female
Genes, Dominant
Genetic Variation
Humans
Lod Score
Male
Middle Aged
Paraplegia--genetics
Pedigree
Phenotype

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