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pro vyhledávání: '"RNaseH qPCR"'
Autor:
David Y, Barefield, Thomas L, Lynch, Aravindakshan, Jagadeesan, Thriveni, Sanagala, Sakthivel, Sadayappan
Publikováno v:
Journal of molecular biomarkers & diagnosis
A 25-basepair deletion variant of MYBPC3 occurs at high frequency in individuals of South Asian descent and is estimated to affect 55 million people worldwide, carrying an increased likelihood of cardiomyopathy. Since this variant is prevalent and se
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::529ede96c61841f88d70848e20fe990c
https://pubmed.ncbi.nlm.nih.gov/27990320
https://pubmed.ncbi.nlm.nih.gov/27990320
Autor:
Barefield DY; Department of Cell and Molecular Physiology, Loyola University, Chicago, USA; Center for Genetic Medicine, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA., Lynch TL 4th; Department of Cell and Molecular Physiology, Loyola University, Chicago, USA., Jagadeesan A; Department of Cell and Molecular Physiology, Loyola University, Chicago, USA., Sanagala T; Department of Cardiology and Echocardiography and Cardiographics, Loyola University, Chicago, USA., Sadayappan S; Department of Cell and Molecular Physiology, Loyola University, Chicago, USA.
Publikováno v:
Journal of molecular biomarkers & diagnosis [J Mol Biomark Diagn] 2016 Nov; Vol. 7 (6). Date of Electronic Publication: 2016 Sep 30.