Associated Papers
Relevance of genetic testing in the gene-targeted trial era: the Rostock Parkinson's disease study.
Westenberger A et al.
Brain : a Journal of Neurology, 2024
39087914 (PubMed )
Supplement: awae188_supplementary_data.zip › awae188_Supplementary_Table_6.f..xlsx › Sheet1
Makorin RING finger protein 3 and central precocious puberty.
Maione L et al.
Current Opinion in Endocrine and Metabolic Research, 2020
Parkin (PARK 2) mutations are rare in Czech patients with early-onset Parkinson's disease.
Fiala O et al.
Plos One, 2014
Parkin mutations and phenotypic features in Czech patients with early-onset Parkinson's disease.
Fiala O et al.
Neuro Endocrinology Letters, 2010
Analysis of Nigerians with apparently sporadic Parkinson disease for mutations in LRRK2, PRKN and ATXN3.
Okubadejo N et al.
Plos One, 2008
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