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Over ons Praktische zaken Waar vindt u ons dr. K.Y. (Kai Yu) Ma

Publicaties

Molecular genetics of monogenic movement disorders: making meaning of rare variants

A Gain-of-Function Variant in Dopamine D2 Receptor and Progressive Chorea and Dystonia Phenotype

Cerebellar developmental deficits underlie neurodegenerative disorder spinocerebellar ataxia type 23

Comparative Studies in the A30P and A53T α-Synuclein C. elegans Strains to Investigate the Molecular Origins of Parkinson's Disease

Parkinson's disease-associated VPS35 mutant reduces mitochondrial membrane potential and impairs PINK1/Parkin-mediated mitophagy

Systematic analysis of PINK1 variants of unknown significance shows intact mitophagy function for most variants

Reply: PLD3 and spinocerebellar ataxia

Crystal structure of truncated human coatomer protein complex subunit ζ1 (Copζ1)

Temporal Multivariate Networks

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