Further evidence that SPG3A gene mutations cause autosomal dominant hereditary spastic paraplegia

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Bibliographic Details
Published in:	Annals of neurology Vol. 51; no. 6; pp. 794 - 795
Main Authors:	Muglia, Maria, Magariello, Angela, Nicoletti, Giuseppe, Patitucci, Alessandra, Gabriele, Anna Lia, Conforti, Francesca Luisa, Mazzei, Rosalucia, Caracciolo, Manuela, Ardito, Bonaventura, Lastilla, Marcello, Tedeschi, Gioacchino, Quattrone, Aldo
Format:	Journal Article
Language:	English
Published:	New York Wiley Subscription Services, Inc., A Wiley Company 01-06-2002
Subjects:	Child Chromosomes, Human, Pair 14 - genetics Genes, Dominant - genetics GTP Phosphohydrolases - genetics GTP-Binding Proteins Humans Italy Membrane Proteins Point Mutation Sequence Analysis, DNA Spastic Paraplegia, Hereditary - genetics Italy
Online Access:	Get full text
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Bibliography:	ArticleID:ANA10185 istex:22E9BD1EEAC7E6C9CF7B22E0D7D74C29717F058B ark:/67375/WNG-P98CM2SB-N SourceType-Other Sources-1 content type line 63 ObjectType-Correspondence-1
ISSN:	0364-5134 1531-8249
DOI:	10.1002/ana.10185