Novel syndromic form of X-linked complicated spastic paraplegia
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference11 articles.
1. X linked spastic paraplegia (SPG2): clinical heterogeneity at a single gene locus.
2. A comprehensive genetic map of the human genome based on 5,264 microsatellites
3. X linked complicated spastic paraplegia, MASA syndrome, and X linked hydrocephalus owing to congenital stenosis of the aqueduct of Sylvius: variable expression of the same mutation at Xq28.
4. X-linked spastic paraplegia: evidence for homogeneity with a variable phenotype
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