Predominant neurological phenotype in a Hungarian family with two novel mutations in the XPA gene—case series
- 期刊名称Neurological Sciences
- 作者Zádori, Dénes; Szpisjak, László; Németh, István Balázs; Reisz, Zita; Kovacs, Gabor G.; Szépfalusi, Noémi; Németh, Viola Luca; Maróti, Zoltán; Tóth-Molnár, Edit; Oláh, Judit; Vécsei, László; Klivényi, Péter; Kalmár, Tibor
- 印刷ISSN1590-1874
- 电子ISSN1590-3478
- 文件大小243.72KB
- 发表时间2019-9-2
- DOI10.1007/s10072-019-04044-6
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