Morphological analysis of 13 LMNA variants identified in a cohort of 324 unrelated patients with idiopathic or familial dilated cardiomyopathy

Autor Cowan, Jason, Li, Duanxiang, Gonzalez-Quintana, Jorge, Morales, Ana, Hershberger, Ray E.
Vydáno 2009

Coding sequence rare variants identified in MYBPC3, MYH6, TPM1, TNNC1 and TNNI3 from 312 patients with familial or idiopathic dilated cardiomyopathy

Autor Hershberger, Ray E., Norton, Nadine, Morales, Ana, Li, Duanxiang, Siegfried, Jill D., Gonzalez-Quintana, Jorge
Vydáno 2010

Identification of Novel Mutations in RBM20 in Patients with Dilated Cardiomyopathy

Autor Li, Duanxiang, Morales, Ana, Gonzalez‐Quintana, Jorge, Norton, Nadine, Siegfried, Jill D., Hofmeyer, Mark, Hershberger, Ray E.
Vydáno 2010

SCN5A Rare Variants in Familial Dilated Cardiomyopathy Decrease Peak Sodium Current Depending on the Common Polymorphism H558R and Common Splice Variant Q1077del

Autor Cheng, Jianding, Morales, Ana, Siegfried, Jill D., Li, Duanxiang, Norton, Nadine, Song, Junyao, Gonzalez‐Quintana, Jorge, Makielski, Jonathan C., Hershberger, Ray E.
Vydáno 2010

Genome-wide Studies of Copy Number Variation and Exome Sequencing Identify Rare Variants in BAG3 as a Cause of Dilated Cardiomyopathy

Autor Norton, Nadine, Li, Duanxiang, Rieder, Mark J., Siegfried, Jill D., Rampersaud, Evadnie, Züchner, Stephan, Mangos, Steve, Gonzalez-Quintana, Jorge, Wang, Libin, McGee, Sean, Reiser, Jochen, Martin, Eden, Nickerson, Deborah A., Hershberger, Ray E.
Vydáno 2011