Genome-wide studies of copy number variation and exome sequencing identify rare variants in BAG3 as a cause of dilated cardiomyopathy
Page 1 of 1
Genome-wide studies of copy number variation and exome sequencing identify rare variants in BAG3 as a cause of dilated cardiomyopathy
Norton N, Li D, Rieder MJ, Siegfried JD, Rampersaud E, Züchner S, Mangos S, Gonzalez-Quintana J, Wang L, McGee S, Reiser J, Martin E, Nickerson DA, Hershberger RE. Genome-wide studies of copy number variation and exome sequencing identify rare variants in BAG3 as a cause of dilated cardiomyopathy. Am J Hum Genet. 2011 Mar 11;88(3):273-82. doi: 10.1016/j.ajhg.2011.01.016. Epub 2011 Feb 25.
Similar topics
» Genome-wide Studies of Copy Number Variation and Exome Sequencing Identify Rare Variants in BAG3 as a Cause of Dilated Cardiomyopathy
» Rare copy number variations in congenital heart disease patients identify unique genes in left-right patterning
» Rare copy number variants analysis identifies novel candidate genes in heterotaxy syndrome patients with congenital heart defects
» Genome-Wide Linkage, Exome Sequencing and Functional Analyses Identify ABCB6 as the Pathogenic Gene of Dyschromatosis Universalis Hereditaria
» Copy-Number Variation Contributes to the Mutational Load of Bardet-Biedl Syndrome
» Rare copy number variations in congenital heart disease patients identify unique genes in left-right patterning
» Rare copy number variants analysis identifies novel candidate genes in heterotaxy syndrome patients with congenital heart defects
» Genome-Wide Linkage, Exome Sequencing and Functional Analyses Identify ABCB6 as the Pathogenic Gene of Dyschromatosis Universalis Hereditaria
» Copy-Number Variation Contributes to the Mutational Load of Bardet-Biedl Syndrome
Page 1 of 1
Permissions in this forum:
You cannot reply to topics in this forum