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Medientyp
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Erscheinungsjahr
Autor/in
- Prokisch, Holger
- Hempel, Maja 3
- Santer, René 2
- Tsiakas, Konstantinos 2
- Aherrahrou, Zouhair 1
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5 Einträge gefunden
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Recurrent acute liver failure in alanyl-tRNA synthetase-1 (AARS1) deficiency
2020 - Forschungsinformationssystem des UKE -
Recessive mutations in >VPS13D cause childhood-onset movement disorders
- Gauthier, Julie
- Meijer, Inge A
- Lessel, Davor
- Mencacci, Niccolò E
- Krainc, Dimitri
- Hempel, Maja
- Tsiakas, Konstantinos
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Genetic variation at chromosome 1p13.3 affects sortilin mRNA expression, cellular LDL-uptake and serum LDL levels which translates to the risk of coronary artery disease.
- Linsel-Nitschke, Patrick
- Heeren, Jörg
- Aherrahrou, Zouhair
- Bruse, Petra
- Gieger, Christian
- Illig, Thomas
- Prokisch, Holger
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Phenotypic spectrum associated with mutations of the mitochondrial polymerase gamma gene.
- Horvath, Rita
- Hudson, Gavin
- Ferrari, Gianfrancesco
- Fütterer, Nancy
- Ahola, Sofia
- Lamantea, Eleonora
- Prokisch, Holger