E. Elert

Expanding the phenotype associated with missense mutations of the ARX gene

E. Obersztyn, A. Charzewska, D. Hoffman-Zacharska, 2013, American journal of medical genetics. Part A.

Screening for the hereditary spastic paraplaegias SPG4 and SPG3A with the multiplex ligation-dependent probe amplification technique in a large population of affected individuals

J. Zaremba, W. Krysa, M. Rajkiewicz, 2013, Neurological Sciences.