SPG11 compound mutations in spastic paraparesis with thin corpus callosum. [electronic resource]
Producer: 20080826Description: 332-6 p. digitalISSN:- 1526-632X
- Adult
- Agenesis of Corpus Callosum
- Child
- Chromosome Disorders -- genetics
- Chromosomes, Human, Pair 15 -- genetics
- Corpus Callosum -- diagnostic imaging
- DNA Mutational Analysis
- Energy Metabolism -- genetics
- Frontal Lobe -- diagnostic imaging
- Gene Frequency
- Genes, Recessive -- genetics
- Genetic Markers -- genetics
- Genetic Predisposition to Disease -- genetics
- Genetic Testing
- Genotype
- Humans
- Intellectual Disability -- complications
- Mutation -- genetics
- Nervous System Malformations -- complications
- Paraparesis, Spastic -- complications
- Proteins -- genetics
- Radionuclide Imaging
- Spain
- Syndrome
- Thalamus -- diagnostic imaging
No physical items for this record
Publication Type: Case Reports; Journal Article
There are no comments on this title.
Log in to your account to post a comment.