Zádori Dénes, Szpisjak László, Németh István Balázs, Reisz Zita, Kovács Gábor Géza, Szépfalusi Noémi, . . . Kalmár Tibor. (2019). Predominant neurological phenotype in a Hungarian family with two novel mutations in the XPA gene-case series.
Chicago Style (17th ed.) CitationZádori Dénes, et al. Predominant Neurological Phenotype in a Hungarian Family with Two Novel Mutations in the XPA Gene-case Series. 2019.
MLA idézésZádori Dénes, et al. Predominant Neurological Phenotype in a Hungarian Family with Two Novel Mutations in the XPA Gene-case Series. 2019.
Figyelem: ezek az hivatkozások nem 100%-ban pontosak..