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Genotypic and phenotypic features in homozygous familial hypercholesterolemia caused by proprotein convertase subtilisin/kexin type 9 (PCSK9) gain-of-function mutation.
Mabuchi H, Nohara A, Noguchi T, Kobayashi J, Kawashiri MA, Inoue T, Mori M, Tada H, Nakanishi C, Yagi K, Yamagishi M, Ueda K, Takegoshi T, Miyamoto S, Inazu A, Koizumi J; Hokuriku FH Study Group. Mabuchi H, et al. Among authors: tada h. Atherosclerosis. 2014 Sep;236(1):54-61. doi: 10.1016/j.atherosclerosis.2014.06.005. Epub 2014 Jun 26. Atherosclerosis. 2014. PMID: 25014035
Whole Exome Sequencing in Monogenic Dyslipidemias.
Tada H, Kawashiri MA, Yamagishi M, Hayashi K. Tada H, et al. J Atheroscler Thromb. 2015;22(9):881-5. doi: 10.5551/jat.ED016. Epub 2015 Apr 24. J Atheroscler Thromb. 2015. PMID: 25911986 Free article. No abstract available.
Significance of Genetic Diagnosis of Familial Hypercholesterolemia.
Kawashiri MA, Tada H, Yamagishi M. Kawashiri MA, et al. Among authors: tada h. J Atheroscler Thromb. 2016 May 2;23(5):554-6. doi: 10.5551/jat.ED038. Epub 2016 Mar 29. J Atheroscler Thromb. 2016. PMID: 27025683 Free article. No abstract available.
1,651 results