REAL

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, 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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Item Type: Article
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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