Altered pituitary morphology as a sign of benign hereditary chorea caused by TITF1/NKX2.1 mutations.

Authors:
Thust S; Veneziano L; Parkinson MH; Bhatia KP; Mantuano E and 3 more

Journal:
Neurogenetics

Publication Year: 2022

DOI:
10.1007/s10048-021-00680-3

PMCID:
PMC8960566

PMID:
35079915

View on PubMed View on PMC View Publisher
Journal Information

Full Title: Neurogenetics

Abbreviation: Neurogenetics

Country: Unknown

Publisher: Unknown

Language: N/A

Publication Details

Subject Category: Neurology

Available in Europe PMC: Yes

Available in PMC: Yes

PDF Available: No

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"Declarations Competing interestsThe authors declare no competing interests. Competing interests The authors declare no competing interests."

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"Funding PG receives funding from the European Friedreich’s Ataxia Consortium for Translational Studies (EFACTS; HEALTH-F2-2010-242193; FP7 Grant). ST, PG, MHP, KB, and ID work at University College London Hospitals/University College London which receives a proportion of its funding from the Department of Health’s National Institute for Health Research Biomedical Research Centres funding scheme. PG is also supported by North Thames CRN UK. This project was part of REC 04/Q0505/21."

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Last Updated: Aug 05, 2025