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Locus heterogeneity, anticipation and reduction of the chromosome 2p minimal candidate region in autosomal dominant familial spastic paraplegia

✍ Scribed by W.K. Scott; P.C. Gaskell; F. Lennon; C.M. Wolpert; M.M. Menold; A.S. Aylsworth; C. Warner; C.D. Farrell; R.-M.N. Boustany; S.G. Albright; E. Boyd; H.M. Kingston; W.J.K. Cumming; J.M. Vance; M.A. Pericak-Vance


Book ID
106257412
Publisher
Springer
Year
1997
Tongue
English
Weight
402 KB
Volume
1
Category
Article
ISSN
1364-6745

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Three dominantly inherited "pure" form of familial spastic paraplegia (FSP) genes have been genetically mapped to regions of chromosomes, yet no specific genes or mutations have been identified (FSPI ; chromosome 14q, FSP2; chromosome 2p and FSP3; chromosome 15q). We studied a "pure" form of autosom