Living‐donor liver transplantation for homozygous familial hypercholesterolemia from a donor with heterozygous hypercholesterolemia

Familial hypercholester‐olemia is a rare inherited disease with an incidence of approximately one per million. Severe hypercholesterolemia is observed from the time of birth onwards. It is associated with severe atherosclerosis in childhood, leading to death from myocardial infarction before the age...

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Veröffentlicht in:Transplant international 2003-04, Vol.16 (4), p.276-279
Hauptverfasser: Shirahata, Yasuhiro, Ohkohchi, Nobuhiro, Kawagishi, Naoki, Syouji, Masaru, Tsukamoto, Sigeki, Sekiguchi, Satoru, Koyamada, Nozomisa, Oikawa, Sinichi, Satomi, Susumu
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