| Title | Authors | Year | Journal |
|---|---|---|---|
| Phenotypic spectrum associated with mutations of the mitochondrial polymerase gamma gene. | Udd B | 2006 | Brain : a journal of neurology |
| Mitochondrial DNA polymerase W748S mutation: a common cause of autosomal recessive ataxia with ancient European origin. | Udd B | 2005 | American journal of human genetics |
| POLG mutations in neurodegenerative disorders with ataxia but no muscle involvement. | Udd B | 2004 | Neurology |
Version:20250429
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