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October 16, 2006Movement Disorders

New syndromic form of benign hereditary chorea is associated with a deletion of TITF‐1 and PAX‐9 contiguous genes

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Authors

DDDavid DevosInsermIVIsabelle VuillaumeABAlix de BecdelièvreInserm

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Devos et al. (2006) studied this question.

synapsesocial.com/papers/69de69a17ed287395e558c2ahttps://doi.org/10.1002/mds.21135
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Also Consider

Synapse has enriched 4 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1A novel TITF-1 mutation causes benign hereditary chorea with response to levodopa2005 · 88 citations
  2. 2Benign hereditary chorea: Clinical, genetic, and pathological findings2003 · 82 citations
  3. 3Benign Familial Chorea With Onset in Childhood1973 · 41 citations
  4. 4Deletion of Thyroid Transcription Factor-1 Gene in an Infant with Neonatal Thyroid Dysfunction and Respiratory Failure1998 · 268 citations