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An SPG3A whole gene deletion neither co-segregates with disease nor modifies phenotype in a hereditary spastic paraplegia family with a pathogenic SPG4 deletion

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Bibliographic Details
Published in:	Neurogenetics 2007-11, Vol.8 (4), p.317-318
Main Authors:	Beetz, Christian, Nygren, Anders O H, Deufel, Thomas, Reid, Evan
Format:	Article
Language:	English
Subjects:	Adenosine Triphosphatases - genetics Adult Child Exons Female Gene Deletion GTP Phosphohydrolases - genetics GTP-Binding Proteins Hereditary spastic paraplegia Humans Male Membrane Proteins Pedigree Phenotype Phenotypes Spastic Paraplegia, Hereditary - genetics Spastin
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