Mutations of the SPG11 gene in patients with autosomal recessive spastic paraparesis and thin corpus callosum. [electronic resource]
Producer: 20080429Description: 607-9 p. digitalISSN:- 1468-330X
- Adolescent
- Adult
- Age of Onset
- Atrophy
- Cerebral Cortex -- pathology
- Chromosome Deletion
- Chromosomes, Human, Pair 15 -- genetics
- Consanguinity
- Corpus Callosum -- pathology
- DNA Mutational Analysis
- Female
- Genes, Recessive -- genetics
- Haplotypes -- genetics
- Humans
- Magnetic Resonance Imaging
- Male
- Microsatellite Repeats -- genetics
- Pedigree
- Phenotype
- Proteins -- genetics
- Spastic Paraplegia, Hereditary -- genetics
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Publication Type: Letter
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