Zádori, Dénes and Szpisjak, László and Németh, István Balázs and Reisz, Zita and Kovács, Gábor Géza and Szepfalusi, Noémi and Németh, Viola Luca and Maróti, Zoltán and Tóth-Molnár, Edit and Oláh, Judit and Vécsei, László and Klivényi, Péter and Kalmár, Tibor (2019) Predominant neurological phenotype in a Hungarian family with two novel mutations in the XPA gene – case series. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. ISSN 1590-3478
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| Item Type: | Article |
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| Subjects: | R Medicine / orvostudomány > RC Internal medicine / belgyógyászat > RC0321 Neuroscience. Biological psychiatry. Neuropsychiatry / idegkórtan, neurológia, pszichiátria |
| Depositing User: | Dr. Dénes Zádori |
| Date Deposited: | 17 Sep 2019 06:40 |
| Last Modified: | 06 Apr 2023 07:22 |
| URI: | http://real.mtak.hu/id/eprint/99613 |
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