Journal
ANNALS OF NEUROLOGY
Volume 54, Issue 6, Pages 796-803Publisher
WILEY
DOI: 10.1002/ana.10768
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We updated the clinical features of a consanguineous Arab Israeli family, in which four of seven children were affected by spastic paraplegia complicated by skin pigmentary abnormalities. A genomewide linkage screen performed for the family identified a new locus (SPG23) for this form of hereditary spastic paraplegia, in an approximately 25cM region of chromosome 1q24-q32, with a peak logarithm of odds score of 3.05.
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