Mice lacking MBNL1 and MBNL2 exhibit sudden cardiac death and molecular signatures recapitulating myotonic dystrophy

KY Lee, C Seah, C Li, YF Chen, CY Chen… - Human Molecular …, 2022 - academic.oup.com
Myotonic dystrophy (DM) is caused by expansions of C (C) TG repeats in the non-coding
regions of the DMPK and CNBP genes, and DM patients often suffer from sudden cardiac …
被引用次数：8 相关文章

Mice lacking MBNL1 and MBNL2 exhibit sudden cardiac death and molecular signatures recapitulating myotonic dystrophy.

KY Lee, C Seah, C Li, YF Chen, CY Chen… - Human Molecular …, 2022 - europepmc.org
Myotonic dystrophy (DM) is caused by expansions of C (C) TG repeats in the non-coding
regions of the DMPK and CNBP genes, and DM patients often suffer from sudden cardiac …

Mice lacking MBNL1 and MBNL2 exhibit sudden cardiac death and molecular signatures recapitulating myotonic dystrophy

KY Lee, C Seah, C Li, YF Chen… - Human molecular …, 2022 - pubmed.ncbi.nlm.nih.gov
Myotonic dystrophy (DM) is caused by expansions of C (C) TG repeats in the non-coding
regions of the DMPK and CNBP genes, and DM patients often suffer from sudden cardiac …

Mice lacking MBNL1 and MBNL2 exhibit sudden cardiac death and molecular signatures recapitulating myotonic dystrophy.

KY Lee, C Seah, C Li, YF Chen… - Human Molecular …, 2022 - search.ebscohost.com
Myotonic dystrophy (DM) is caused by expansions of C (C) TG repeats in the non-coding
regions of the DMPK and CNBP genes, and DM patients often suffer from sudden cardiac …
[PDF] archive.org

[PDF][PDF] Mice Lacking MBNL1 and MBNL2 Exhibit Sudden Cardiac Death and Molecular Signatures Recapitulating Myotonic Dystrophy

KY Lee, C Seah, C Li, YF Chen, CY Chen, CI Wu… - 2022 - scholar.archive.org
Myotonic dystrophy (DM) is caused by expansions of C (C) TG repeats in the non-coding
regions of the DMPK and CNBP genes, and DM patients often suffer from sudden cardiac …
[PDF] oup.com

[PDF][PDF] Mice lacking MBNL1 and MBNL2 exhibit sudden cardiac death and molecular signatures recapitulating myotonic dystrophy

KY Lee, C Seah, C Li, YF Chen, CY Chen… - Human Molecular …, 2022 - academic.oup.com
Myotonic dystrophy (DM) is caused by expansions of C (C) TG repeats in the non-coding
regions of the DMPK and CNBP genes, and DM patients often suffer from sudden cardiac …
[HTML] nih.gov

[HTML][HTML] Mice lacking MBNL1 and MBNL2 exhibit sudden cardiac death and molecular signatures recapitulating myotonic dystrophy

KY Lee, C Seah, C Li, YF Chen, CY Chen… - Human Molecular …, 2022 - ncbi.nlm.nih.gov
Myotonic dystrophy (DM) is caused by expansions of C (C) TG repeats in the non-coding
regions of the DMPK and CNBP genes, and DM patients often suffer from sudden cardiac …

Mice lacking MBNL1 and MBNL2 exhibit sudden cardiac death and molecular signatures recapitulating myotonic dystrophy

KY Lee, C Seah, C Li, YF Chen, CY Chen… - Human Molecular …, 2022 - pure.lib.cgu.edu.tw
Myotonic dystrophy (DM) is caused by expansions of C (C) TG repeats in the non-coding
regions of the DMPK and CNBP genes, and DM patients often suffer from sudden cardiac …

Mice lacking MBNL1 and MBNL2 exhibit sudden cardiac death and molecular signatures recapitulating myotonic dystrophy

KY Lee, C Seah, C Li, YF Chen, CY Chen… - Human Molecular …, 2022 - pure.lib.cgu.edu.tw
摘要Myotonic dystrophy (DM) is caused by expansions of C (C) TG repeats in the non-
coding regions of the DMPK and CNBP genes, and DM patients often suffer from sudden …