PCSK9 acts as a chaperone for the LDL receptor in the endoplasmic reticulum
Thea Bismo Strøm(Oslo University Hospital), Trond P. Leren(Oslo University Hospital), Kristian Tveten(Telemark Hospital)
Cited by 46
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