Löfgren A
Publications:
| Title | Authors | Year | Journal |
|---|---|---|---|
| A novel POLG gene mutation in 4 children with Alpers-like hepatocerebral syndromes. | Löfgren A | 2010 | Archives of neurology |
| POLG mutations in neurodegenerative disorders with ataxia but no muscle involvement. | Löfgren A | 2004 | Neurology |
| Novel POLG mutations in progressive external ophthalmoplegia mimicking mitochondrial neurogastrointestinal encephalomyopathy. | Löfgren A | 2003 | European journal of human genetics : EJHG |
| Recessive POLG mutations presenting with sensory and ataxic neuropathy in compound heterozygote patients with progressive external ophthalmoplegia. | Löfgren A | 2003 | Neuromuscular disorders : NMD |
| Patient homozygous for a recessive POLG mutation presents with features of MERRF. | Löfgren A | 2003 | Neurology |
| Mutation of POLG is associated with progressive external ophthalmoplegia characterized by mtDNA deletions. | Löfgren A | 2001 | Nature genetics |
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