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Iron overload is accompanied by mitochondrial and lysosomal dysfunction in WDR45 mutant cells
2018 - Forschungsinformationssystem des UKE
Recessive mutations in >VPS13D cause childhood-onset movement disorders
2018 - Forschungsinformationssystem des UKE
Pathogenic effects of novel mutations in the P-type ATPase ATP13A2 (PARK9) causing Kufor-Rakeb syndrome, a form of early-onset parkinsonism.
2011 - Forschungsinformationssystem des UKE