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POLG2, 24-BP INS, NT1207

National Institutes of Health

Related topics

Related topics

1 relation
VARIANT OF UNKNOWN SIGNIFICANCE

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2010
2010
Late-onset ptosis and myopathy in a patient with a heterozygous insertion in POLG2 Maggie C. WalterBirgit CzerminSolvig Muller-ZiermannStefanie BulstJoanna D. Stewart • Gavin HudsonPeter…
Polymerase gamma 1 (POLG) mutations are a frequent cause of both autosomal dominant and recessive complex neurological phenotypes… 
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