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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
PaperCitations, authors & open-access status
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. ScholarIQ records 127 citations, 2012 year and closed oa status.
127
Citations
2012
Year
closed
OA Status