familial hypercholesterolemia syndrome 范
Familial Hypercholesterolemia FH 家族性高胆固醇血症
familial hypercholesterolemia 家族性高胆甾醇血症
homozygote familial hypercholesterolemia 纯合子家族性高胆固醇血症
homozygous familial hypercholesterolemia 纯合子家族性高胆固醇血症
familial hypercholesterolemia-like phenotype 家族性高胆固醇血症样表型
familial hypercholesterolemia like phenotype 家族性高胆固醇血症样表型
Molecular Studies of Familial Hypercholesterolemia 家族性高胆固醇血症疾病基因的分生研究
It is called familial "hypercholesterolemia" and can play a role in 1 of 500 people.
这就是所谓家族“高胆固醇血症”和可以发挥作用，1 500人。
For instance, familial hypercholesterolemia (FH) typically results from mutations in LDLR encoding the low-density lipoprotein (LDL) receptor.
例如，家族性血胆脂醇过多症(FH)通常起源于编码低密度脂蛋白(LDL)受体的LDLR突变。
Objective: To study the pathogenesis of a homozygous patient with familial hypercholesterolemia.
目的：研究家族性高胆固醇血症纯合子患者的发病机理。
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