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

Zádori Dénes and Szpisjak László and Németh István Balázs and Reisz Zita and Kovács Gábor Géza and Szépfalusi Noémi and Németh Viola Luca and Maróti Zoltán and Tóth-Molnár Edit and Oláh Judit and Vécsei László and Klivényi Péter and 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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Creators:
Zádori Dénes MTMT
Szpisjak László MTMT
Németh István Balázs MTMT
Reisz Zita MTMT
Kovács Gábor Géza MTMT
Szépfalusi Noémi
Németh Viola Luca MTMT
Maróti Zoltán MTMT
Tóth-Molnár Edit MTMT
Oláh Judit
Vécsei László MTMT
Klivényi Péter MTMT
Kalmár Tibor MTMT
Item Type: Journal Article
Journal or Publication Title: NEUROLOGICAL SCIENCES
Date: 2019
Volume: 41
Number: 1
Page Range: pp. 125-129
ISSN: 1590-1874
Faculty/Unit: Faculty of Medicine
Institution: University of Szeged (2000-)
Language: English
MTMT rekordazonosító: 30834531
DOI azonosító: 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
Web of Science® Times Cited: 5 View citing articles in Web of Science®

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