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First cases in the Czech Republic of the Hallervorden-Spatz disease resulting from mutation in the pantothenate kinase 2 gene.
Neuro Endocrinol Lett. 2005 Jun;26(3):213-8.
Neuro Endocrinol Lett. 2005.
PMID: 15990724
Two types of recessive hereditary spastic paraplegia in Roma patients in compound heterozygous state; no ethnically prevalent variant found.
Meszarosova AU, Seeman P, Jencik J, Drabova J, Cibochova R, Stellmachova J, Safka Brozkova D.
Meszarosova AU, et al. Among authors: cibochova r.
Neurosci Lett. 2020 Mar 16;721:134800. doi: 10.1016/j.neulet.2020.134800. Epub 2020 Jan 30.
Neurosci Lett. 2020.
PMID: 32007496
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