Found: 4
Select item for more details and to access through your institution.
A clinical, genetic and biochemical study of SPG7 mutations in hereditary spastic paraplegia.
- Published in:
- Brain: A Journal of Neurology, 2004, v. 127, n. 9, p. 2148, doi. 10.1093/brain/awh299
- By:
- Publication type:
- Article
Screening of patients with hereditary spastic paraplegia reveals seven novel mutations in the SPG4 (Spastin) gene.
- Published in:
- Human Mutation, 2003, v. 21, n. 2, p. 170, doi. 10.1002/humu.9108
- By:
- Publication type:
- Article
correction: The deoxyguanosine kinase gene is mutated in individuals with depleted hepatocerebral mitochondrial DNA.
- Published in:
- 2001
- By:
- Publication type:
- Erratum
Homozygosity at chromosome 8qter in individuals affected by mal de Meleda (Meleda disease) originating from the island of Meleda.
- Published in:
- British Journal of Dermatology, 2001, v. 144, n. 4, p. 731, doi. 10.1046/j.1365-2133.2001.04127.x
- By:
- Publication type:
- Article