Benign hereditary chorea: phenotype, prognosis, therapeutic outcome and long term follow-up in a large series with new mutations in the<i>TITF1/NKX2-1</i>gene
Benign hereditary chorea: phenotype, prognosis, therapeutic outcome and long term follow-up in a large series with new mutations in the<i>TITF1/NKX2-1</i>gene is a paper indexed in ScholarIQ from OpenAlex.
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Benign hereditary chorea: phenotype, prognosis, therapeutic outcome and long term follow-up in a large series with new mutations in the<i>TITF1/NKX2-1</i>gene has 127 citations in the OpenAlex counts ScholarIQ stores.
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Benign hereditary chorea: phenotype, prognosis, therapeutic outcome and long term follow-up in a large series with new mutations in the<i>TITF1/NKX2-1</i>gene has 2012 year in the ScholarIQ index.
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