Modeling structural and functional deficiencies of RBM20 familial dilated cardiomyopathy using human induced pluripotent stem cells
Dilated cardiomyopathy (DCM) is a leading cause of heart failure. In families with autosomal-
dominant DCM, heterozygous missense mutations were identified in RNA-binding motif …
dominant DCM, heterozygous missense mutations were identified in RNA-binding motif …
[PDF][PDF] Modeling structural and functional deficiencies of RBM20 familial dilated cardiomyopathy using human induced pluripotent stem cells
SP Wyles, X Li, SC Hrstka, S Reyes… - Human Molecular …, 2015 - researchgate.net
Dilated cardiomyopathy (DCM) is a leading cause of heart failure. In families with autosomal-
dominant DCM, heterozygous missense mutations were identified in RNA-binding motif …
dominant DCM, heterozygous missense mutations were identified in RNA-binding motif …
Modeling structural and functional deficiencies of RBM20 familial dilated cardiomyopathy using human induced pluripotent stem cells.
SP Wyles, X Li, SC Hrstka, S Reyes… - Human Molecular …, 2016 - search.ebscohost.com
Dilated cardiomyopathy (DCM) is a leading cause of heart failure. In families with autosomal-
dominant DCM, heterozygous missense mutations were identified in RNA-binding motif …
dominant DCM, heterozygous missense mutations were identified in RNA-binding motif …
Modeling structural and functional deficiencies of RBM20 familial dilated cardiomyopathy using human induced pluripotent stem cells.
SP Wyles, X Li, SC Hrstka, S Reyes… - Human Molecular …, 2015 - europepmc.org
Dilated cardiomyopathy (DCM) is a leading cause of heart failure. In families with autosomal-
dominant DCM, heterozygous missense mutations were identified in RNA-binding motif …
dominant DCM, heterozygous missense mutations were identified in RNA-binding motif …
Modeling structural and functional deficiencies of RBM20 familial dilated cardiomyopathy using human induced pluripotent stem cells
SP Wyles, X Li, SC Hrstka, S Reyes… - Human …, 2016 - mayoclinic.elsevierpure.com
Dilated cardiomyopathy (DCM) is a leading cause of heart failure. In families with autosomal-
dominant DCM, heterozygous missense mutations were identified in RNA-binding motif …
dominant DCM, heterozygous missense mutations were identified in RNA-binding motif …
[HTML][HTML] Modeling structural and functional deficiencies of RBM20 familial dilated cardiomyopathy using human induced pluripotent stem cells
SP Wyles, X Li, SC Hrstka, S Reyes… - Human Molecular …, 2016 - ncbi.nlm.nih.gov
Dilated cardiomyopathy (DCM) is a leading cause of heart failure. In families with autosomal-
dominant DCM, heterozygous missense mutations were identified in RNA-binding motif …
dominant DCM, heterozygous missense mutations were identified in RNA-binding motif …
[引用][C] Modeling structural and functional deficiencies ofRBM20familial dilated cardiomyopathy using human induced pluripotent stem cells
SP Wyles, X Li, SC Hrstka, S Reyes… - Human Molecular …, 2015 - cir.nii.ac.jp
Modeling structural and functional deficiencies of<i>RBM20</i>familial dilated cardiomyopathy
using human induced pluripotent stem cells | CiNii Research CiNii 国立情報学研究所 学術情報 …
using human induced pluripotent stem cells | CiNii Research CiNii 国立情報学研究所 学術情報 …
Modeling structural and functional deficiencies of RBM20 familial dilated cardiomyopathy using human induced pluripotent stem cells
SP Wyles, X Li, SC Hrstka, S Reyes… - Human molecular …, 2016 - pubmed.ncbi.nlm.nih.gov
Dilated cardiomyopathy (DCM) is a leading cause of heart failure. In families with autosomal-
dominant DCM, heterozygous missense mutations were identified in RNA-binding motif …
dominant DCM, heterozygous missense mutations were identified in RNA-binding motif …
Modeling structural and functional deficiencies of RBM20 familial dilated cardiomyopathy using human induced pluripotent stem cells.
SP Wyles, X Li, SC Hrstka, S Reyes… - Human Molecular …, 2015 - europepmc.org
Dilated cardiomyopathy (DCM) is a leading cause of heart failure. In families with autosomal-
dominant DCM, heterozygous missense mutations were identified in RNA-binding motif …
dominant DCM, heterozygous missense mutations were identified in RNA-binding motif …