Homozygous Familial Hypercholesterolemia

Familial hypercholesterolemia (FH) is an inherited disorder with retarded clearance of plasma LDL caused by mutations of the genes involved in the LDL receptor-mediated pathway and most of them exhibit autosomal dominant inheritance. Homozygotes of FH (HoFH) may have plasma LDL-C levels, which are a...

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Bibliografische gegevens
Gepubliceerd in:J Atheroscler Thromb
Hoofdauteurs: Nohara, Atsushi, Tada, Hayato, Ogura, Masatsune, Okazaki, Sachiko, Ono, Koh, Shimano, Hitoshi, Daida, Hiroyuki, Dobashi, Kazushige, Hayashi, Toshio, Hori, Mika, Matsuki, Kota, Minamino, Tetsuo, Yokoyama, Shinji, Harada-Shiba, Mariko
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Japan Atherosclerosis Society 2021
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Review
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC8265428/
https://ncbi.nlm.nih.gov/pubmed/33867421
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5551/jat.RV17050
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