Literature DB >> 15596602

Beginning to understand hereditary spastic paraplegia atlastin.

Jeffrey L Elliott.   

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Year:  2004        PMID： 15596602     DOI： 10.1001/archneur.61.12.1842

Source DB:  PubMed          Journal:  Arch Neurol        ISSN： 0003-9942


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  1 in total

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

Authors:  Christian Beetz; Anders O H Nygren; Thomas Deufel; Evan Reid
Journal:  Neurogenetics       Date:  2007-07-27       Impact factor: 3.017
  1 in total

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