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POLG2, 24-BP INS, NT1207
National Institutes of Health
VARIANT OF UNKNOWN SIGNIFICANCE
Semantic Scholar uses AI to extract papers important to this topic.
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…
M. C. Walters
J. D. StewartG
Corpus ID: 203874235
Polymerase gamma 1 (POLG) mutations are a frequent cause of both autosomal dominant and recessive complex neurological phenotypes…
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