Balicza, Péter and Grosz, Zoltán and Molnár, Viktor and Illés, Anett and Csabán, Dóra and Gézsi, András and Dézsi, Lívia and Zádori, Dénes and Vécsei, László and Molnár, Mária Judit (2018) NKX2-1 New Mutation Associated With Myoclonus, Dystonia, and Pituitary Involvement. FRONTIERS IN GENETICS, 9. pp. 1-5. ISSN 1664-8021
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Official URL: https://doi.org/10.3389/fgene.2018.00335
Item Type: | Article |
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Uncontrolled Keywords: | FAMILY; GENE; TRANSCRIPTION FACTOR; empty sella; PITUITARY; myoclonus dystonia; CHOREA; brain-lung-thyroid syndrome; benign hereditary chorea; NKX2-1 related disorders; NKX2-1 gene |
Subjects: | R Medicine / orvostudomány > RC Internal medicine / belgyógyászat > RC0321 Neuroscience. Biological psychiatry. Neuropsychiatry / idegkórtan, neurológia, pszichiátria |
SWORD Depositor: | MTMT SWORD |
Depositing User: | MTMT SWORD |
Date Deposited: | 17 Sep 2018 08:32 |
Last Modified: | 17 Sep 2018 08:32 |
URI: | http://real.mtak.hu/id/eprint/84149 |
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