Genotypic and phenotypic features in homozygous familial hypercholesterolemia caused by proprotein convertase subtilisin/kexin type 9 (PCSK9) gain-of-function mutation
Hiroshi Mabuchi(Kanazawa University), Junji Koizumi(Kanazawa University), Chiaki Nakanishi(Kanazawa University), Masa‐aki Kawashiri(Kanazawa University), Junji Kobayashi(Chiba University), Mika Mori(Kanazawa University), Kousei Ueda(Komatsu (Japan)), Susumu Miyamoto(Kyoto University Hospital), Atsushi Nohara(Kanazawa University), Tadayoshi Takegoshi(Uwajima City Hospital), Masakazu Yamagishi, Takeshi Inoue(Nara Medical University), Hayato Tada(Kanazawa University), Akihiro Inazu(Kanazawa University), Tohru Noguchi(Kanazawa University), Kunimasa Yagi(University of Ulsan)
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