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Predominant neurological phenotype in a Hungarian family with two novel mutations in the XPA gene-case series

Zádori, Dénes, Szpisjak, László, Németh, István Balázs, Reisz, Zita, Kovács, Gábor Géza, Szépfalusi, Noémi, Németh, Viola Luca, Maróti, Zoltán, Tóth-Molnár, Edit, Oláh, Judit, Vécsei, László, Klivényi, Péter, Kalmár, Tibor: Predominant neurological phenotype in a Hungarian family with two novel mutations in the XPA gene-case series.
NEUROLOGICAL SCIENCES, 41 (1). pp. 125-129. ISSN 1590-1874 (2019)

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Item Type: Article
Journal or Publication Title: NEUROLOGICAL SCIENCES
Date: 2019
Volume: 41
Number: 1
Page Range: pp. 125-129
ISSN: 1590-1874
Faculty: Faculty of Medicine
Institution: Szegedi Tudományegyetem
MTMT id: 30834531
DOI id: https://doi.org/10.1007/s10072-019-04044-6
Date Deposited: 2019. Nov. 08. 14:50
Last Modified: 2020. Jan. 20. 15:44
URI: http://publicatio.bibl.u-szeged.hu/id/eprint/17350

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