Narrowing of the critical region in autosomal recessive spastic paraplegia linked to the SPG5 locus-Reference-Cited by-同舟云学术

Narrowing of the critical region in autosomal recessive spastic paraplegia linked to the SPG5 locus

Published:2003-12-05 Issue:1 Volume:5 Page:49-54
ISSN:1364-6745
Container-title:Neurogenetics
language:en
Short-container-title:Neurogenetics

Author:

Muglia M.,Criscuolo C.,Magariello A.,De Michele G.,Scarano V.,D’Adamo P.,Ambrosio G.,Gabriele A. L.,Patitucci A.,Mazzei R.,Conforti F. L.,Sprovieri T.,Morgante L.,Epifanio A.,La Spina P.,Valentino P.,Gasparini P.,Filla A.,Quattrone A.

Publisher

Springer Science and Business Media LLC

Subject

Cellular and Molecular Neuroscience,Genetics(clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/s10048-003-0167-7.pdf

Reference26 articles.

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2. Hazan J, Lamy C, Melki J, Munnich A, Recondo J de, Weissenbach J (1993) Autosomal dominant familial spastic paraplegia is genetically heterogeneous and one locus maps to chromosome 14q. Nat Genet 5:163–167

3. Hentati A, Perick-Vance M, Lennon F, Wasserman B, Hentati F, Juneja T, Angrist M, Hung W, Boustany R, Bohlega S, Iqbal Z, Huether C, Ben Hamida M, Siddique T (1994) Linkage of a new locus for autosomal dominant familial spastic paraplegia to chromosome 2p. Hum Mol Genet 3:1569–1573

4. Fink JK, Brocade Wu C, Jones SM, Sharp G, Lange B, Lesicki A, Reinglass T, Varvil T, Otterud B, Leppert M (1995) Autosomal dominant familial spastic paraplegia: tight linkage to chromosome 15q. Am J Hum Genet 56:188–192

5. Hedera P, Rainier S, Alvarado D, Zhao X, Williamson J, Otterud B, Leppert M, Fink J (1999) Novel locus for autosomal dominant hereditary spastic paraplegia on chromosome 8q. Am J Hum Genet 64:563–569

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