X. Pan

Functional Characterization of Two Low-Density Lipoprotein Receptor Gene Mutations in Two Chinese Patients with Familial Hypercholesterolemia

Shengyuan Xu, Liyuan Sun, Haihong Wang, 2014, PloS one.

Extremely severe aortic stenosis developed in a young female patient with underdiagnosis of homozygous familial hypercholesterolemia: An 8-year follow-up.

L. Tang, Long Jiang, Luya Wang, 2016, International journal of cardiology.

Functional analysis of low‐density lipoprotein receptor in homozygous familial hypercholesterolemia patients with novel 1439 C→T mutation of low‐density lipoprotein receptor gene

Shu Liu, Zhi-Sheng Jiang, Luya Wang, 2008, Chinese medical journal.

A novel mutation in proprotein convertase subtilisin/kexin type 9 gene leads to familial hypercholesterolemia in a Chinese family.

Shu Liu, Zhi-Sheng Jiang, Luya Wang, 2010, Chinese medical journal.

Seven-year clinical follow-up of a Chinese homozygous familial hypercholesterolemia child with premature xanthomas and coronary artery disease--a need for early diagnosis and aggressive treatment.

F. Gao, Q. Wang, Long Jiang, 2014, International journal of cardiology.

A novel mutation of the LDL receptor gene leading to familial hypercholesterolemia

Ying-Jia Xu, Zhao-su Wu, Luya Wang, 2009 .

Use of Targeted Exome Sequencing in Genetic Diagnosis of Chinese Familial Hypercholesterolemia

X. Pan, Li-yuan Sun, Shi-Wei Yang, 2014, PloS one.