Walleczek NK

References (1)

Title : Treatment of volanesorsen in a patient with familial chylmicronaemia syndrome (FCS) due to homozygous c.337T>C(p.TRP113ARG) - mutation and impact of dietary incompliance: A case report - De Gier_2022_Atherosclerosis_355_65
Author(s) : De Gier C , Skacel G , Walleczek NK , Lischka J , Baumgartner M , Greber-Platzer S
Ref : Atherosclerosis , 355 :65 , 2022
Abstract :
PubMedSearch : De Gier_2022_Atherosclerosis_355_65
PubMedID:
Gene_locus related to this paper: human-LPL