Autosomal recessive hereditary spastic paraplegia type SPG35 due to a novel variant in the FA2H gene in a Czech patientAnna Uhrová Mészárosová, Pavel Seeman, Dana Šafka Brožková et al.|Journal of Clinical Neuroscience|2018Cited by 5
ErratumJudith Stoklasova, D Zemková, Marina Vakaki et al.|Hormone Research in Paediatrics|2016Cited by 0