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Clinical Spectrum of Kufor-Rakeb Syndrome in the Chilean Kindred with ATP13A2 MutationsBEHRENS, Maria I; BRÜGGEMANN, Norbert; HAHNEN, Eric et al.Movement disorders. 2010, Vol 25, Num 12, pp 1929-1937, issn 0885-3185, 9 p.Article

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Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPaseRAMIREZ, Alfredo; HEIMBACH, André; AL-DIN, Amir et al.Nature genetics. 2006, Vol 38, Num 10, pp 1184-1191, issn 1061-4036, 8 p.Article