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Löfgren A

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This page provides a summary of the entries in Polbase associated with this author.

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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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