Found: 3
Select item for more details and to access through your institution.
Analysis of heavy neurofilament subunit gene polymorphism in Russian patients with sporadic motor neuron disease (MND).
- Published in:
- 2004
- By:
- Publication type:
- Report
CuZn-superoxide dismutase gene in sporadic amyotrophic lateral sclerosis patients from Russia: Asp90Ala (D90A) mutation and novel rare polymorphism IVS3+35 A>C.
- Published in:
- Human Mutation, 2000, v. 16, n. 3, p. 277, doi. 10.1002/1098-1004(200009)16:3<277::AID-HUMU27>3.0.CO;2-P
- By:
- Publication type:
- Article
A common 3-bp deletion in the DYT1 gene in Russian families with early-onset torsion dystonia.
- Published in:
- Human Mutation, 1999, v. 14, n. 3, p. 269, doi. 10.1002/(SICI)1098-1004(1999)14:3<269::AID-HUMU12>3.0.CO;2-9
- By:
- Publication type:
- Article