Independent Severe Cases of Heterozygous Familial Hypercholesterolemia Caused by the W483X and Novel W483G Mutations in the Low-Density Lipoprotein Receptor Gene That Were Clinically Diagnosed as Homozygous Cases

scientific article published on 01 June 2019

Independent Severe Cases of Heterozygous Familial Hypercholesterolemia Caused by the W483X and Novel W483G Mutations in the Low-Density Lipoprotein Receptor Gene That Were Clinically Diagnosed as Homozygous Cases is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1089/GTMB.2019.0012
P698PubMed publication ID31161821

P2093author name stringYang Gao
Yue Wu
Hong Shang
Minghui An
Xiaoxu Han
Shitong Cheng
Luya Wang
Wenhui Wen
P2860cites workPredicting the functional impact of protein mutations: application to cancer genomicsQ35224321
P433issue6
P921main subjecthomozygosityQ114049690
heterozygosityQ124059385
familial hypercholesterolemiaQ2711291
P304page(s)401-408
P577publication date2019-06-01
P1433published inGenetic Testing and Molecular BiomarkersQ15753742
P1476titleIndependent Severe Cases of Heterozygous Familial Hypercholesterolemia Caused by the W483X and Novel W483G Mutations in the Low-Density Lipoprotein Receptor Gene That Were Clinically Diagnosed as Homozygous Cases
P478volume23

Search more.