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Q34136479-F76C092A-71BF-40A3-AE09-0E22038F4A9F
Q34136479-F76C092A-71BF-40A3-AE09-0E22038F4A9F
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34136479-F76C092A-71BF-40A3-AE09-0E22038F4A9F
A novel de novo mutation of the TITF1/NKX2-1 gene causing ataxia, benign hereditary chorea, hypothyroidism and a pituitary mass in a UK family and review of the literature.
P2860
Q34136479-F76C092A-71BF-40A3-AE09-0E22038F4A9F
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34136479-F76C092A-71BF-40A3-AE09-0E22038F4A9F
rank
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type
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Statement
wasDerivedFrom
f843a590fa5312d5d14b20a21d55c6411833197e
P2860
Partial deficiency of thyroid transcription factor 1 produces predominantly neurological defects in humans and mice