Autosomal recessive hereditary spastic paraplegia type SPG35 due to a novel variant in the FA2H gene in a Czech patient
Uhrova Meszarosova, Anna, Safka Brozkova, Dana, Vyhnalek, Martin, Mazanec, Radim, Lastuvkova, Jana, Trkova, Marie, Bittoova, Martina, Soldatova, Inna, Seeman, PavelLanguage:
english
Journal:
Journal of Clinical Neuroscience
DOI:
10.1016/j.jocn.2018.10.094
Date:
November, 2018
File:
PDF, 473 KB
english, 2018