Mutations inTITF1 are not relevant to sporadic and familial chorea of unknown cause
Author:
Publisher
Wiley
Subject
Clinical Neurology,Neurology
Reference6 articles.
1. Mutations in TITF-1 are associated with benign hereditary chorea
2. Benign hereditary chorea: Clinical, genetic, and pathological findings
3. Partial deficiency of Thyroid transcription factor 1 produces predominantly neurological defects in humans and mice
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5. Benign hereditary chorea?Entity or syndrome?
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1. Diagnostic Uncertainties: Chorea;Seminars in Neurology;2023-02
2. Chorea: An Update on Genetics;European Neurology;2022
3. Deletion of conserved non‐coding sequences downstream from NKX2‐1 : A novel disease‐causing mechanism for benign hereditary chorea;Molecular Genetics & Genomic Medicine;2021-03-05
4. Recent advances in genetics of chorea;Current Opinion in Neurology;2016-08
5. ADCY5mutations are another cause of benign hereditary chorea;Neurology;2015-06-17
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