NKX2-1 new mutation associated with myoclonus, dystonia, and pituitary involvement

Balicza Péter and Grosz Zoltán and Molnár Viktor and Illés Anett and Csabán Dóra and Gézsi András and Dézsi Livia and Zádori Dénes and Vécsei László and Molnár Mária Judit: NKX2-1 new mutation associated with myoclonus, dystonia, and pituitary involvement.
FRONTIERS IN GENETICS, 9. Terjedelem: 5 p.-Azonosító: 335. (2018)

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Item Type: Journal Article
Journal or Publication Title: FRONTIERS IN GENETICS
Date: 2018
Volume: 9
Page Range: Terjedelem: 5 p.-Azonosító: 335
Faculty/Unit: Faculty of Medicine
Institution: Szegedi Tudományegyetem
Language: English
MTMT rekordazonosító: 3405393
DOI azonosító: https://doi.org/10.3389/fgene.2018.00335
Date Deposited: 2018. Sep. 22. 16:00
Last Modified: 2018. Sep. 22. 16:00
URI: http://publicatio.bibl.u-szeged.hu/id/eprint/13902
Web of Science® Times Cited: 11 View citing articles in Web of Science®

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