A new locus for dominant hereditary spastic paraplegia maps to chromosome 2p12
✍ Scribed by Stephan Züchner; Melanie E. Kail; Martha A. Nance; Perry C. Gaskell; Ingrid K. Svenson; Douglas A. Marchuk; Margaret A. Pericak-Vance; Allison E. Ashley-Koch
- Publisher
- Springer
- Year
- 2006
- Tongue
- English
- Weight
- 162 KB
- Volume
- 7
- Category
- Article
- ISSN
- 1364-6745
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Hereditary spastic paraplegia is a clinically and genetically heterogeneous disorder characterized by progressive spasticity of the lower limbs. Seven loci for autosomal dominant pure hereditary spastic paraplegia (ADPHSP) have already been mapped on chromosomes 14q, 2p, 15q, 8p, 12q, 19q, and 2q. W
## Abstract The hereditary spastic paraplegias (HSPs) are a group of clinically and genetically heterogeneous disorders characterized by progressive lower‐limb spasticity. In this study, we performed linkage analysis on an autosomal recessive pure HSP family and mapped the disease to chromosome 10q