Alexej Knaus
0000-0003-0366-0533
5 papers found
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PSMC3 proteasome subunit variants are associated with neurodevelopmental delay and type I interferon production
A CRISPR-Cas9–engineered mouse model for GPI-anchor deficiency mirrors human phenotypes and exhibits hippocampal synaptic dysfunctions
Complement and inflammasome overactivation mediates paroxysmal nocturnal hemoglobinuria with autoinflammation
Mutations in PIGU Impair the Function of the GPI Transamidase Complex, Causing Severe Intellectual Disability, Epilepsy, and Brain Anomalies
PEDIA: prioritization of exome data by image analysis
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