doi: 10.1007/s10048-007-0099-8.
Epub 2007 Jul 27.
An SPG3A whole gene deletion neither co-segregates with disease nor modifies phenotype in a hereditary spastic paraplegia family with a pathogenic SPG4 deletion
- PMID: 17657515
- DOI: 10.1007/s10048-007-0099-8
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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
Neurogenetics.
2007 Nov.
No abstract available
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