Majamaa K
Publications:
| Title | Authors | Year | Journal |
|---|---|---|---|
| Parkinsonism, premature menopause, and mitochondrial DNA polymerase gamma mutations: clinical and molecular genetic study. | Majamaa K | Lancet | |
| Digenic mutations in severe myoclonic epilepsy of infancy. | Majamaa K | 2009 | Epilepsy research |
| Homozygous W748S mutation in the POLG1 gene in patients with juvenile-onset Alpers syndrome and status epilepticus. | Majamaa K | 2008 | Epilepsia |
| Parkinsonism associated with the homozygous W748S mutation in the POLG1 gene. | Majamaa K | 2008 | Parkinsonism & related disorders |
| Mitochondrial DNA polymerase W748S mutation: a common cause of autosomal recessive ataxia with ancient European origin. | Majamaa K | 2005 | American journal of human genetics |
Showing 1 to 5 of 5 entries