| Title : A Case of Familial Chylomicronemia Syndrome Caused by a Novel Homozygous GPIHBP1 Mutation Successfully Treated with the Selective PPARalpha Modulator Pemafibrate - Otsuki_2026_J.Atheroscler.Thromb__ |
| Author(s) : Otsuki T , Chung Y , Kawachi Y , Komuku S , Yamanishi M , Takano T , Yamaguchi A , Hanada H , Masuda D , Miyashita K , Yamashita S |
| Ref : J Atheroscler Thromb , : , 2026 |
| Abstract : |
| PubMedSearch : Otsuki_2026_J.Atheroscler.Thromb__ |
| PubMedID: 42309774 |