PCSK9-mediated degradation of the LDL receptor generates a 17 kDa C-terminal LDL receptor fragment
Kristian Tveten(Telemark Hospital), Trond P. Leren(Oslo University Hospital), Thea Bismo Str⊘m, Knut Erik Berge
Cited by 37
Related Papers
De Novo Mutations in Protein Kinase Genes CAMK2A and CAMK2B Cause Intellectual Disability
|The American Journal of Human Genetics|2017|202
Calmodulin mutations and life-threatening cardiac arrhythmias: insights from the International Calmodulinopathy Registry
|European Heart Journal|2019|188
Clinical exome sequencing reveals locus heterogeneity and phenotypic variability of cohesinopathies
|Genetics in Medicine|2018|91
Next-generation sequencing of the monogenic obesity genes LEP , LEPR , MC4R , PCSK1 and POMC in a Norwegian cohort of patients with morbid obesity and normal weight controls
|Molecular Genetics and Metabolism|2017|68
De novo substitutions of TRPM3 cause intellectual disability and epilepsy
|European Journal of Human Genetics|2019|68