Rare variant mutations identified in pediatric patients with dilated cardiomyopathy

Những quyển sách tương tự

• Evaluating pathogenicity of rare variants from dilated cardiomyopathy in the exome era
  Bằng: Norton, Nadine, et al.
  Được phát hành: (2012)
• Functional Characterization of TNNC1 Rare Variants Identified in Dilated Cardiomyopathy
  Bằng: Pinto, Jose Renato, et al.
  Được phát hành: (2011)
• Rare variant mutations in pregnancy-associated or peripartum cardiomyopathy
  Bằng: Morales, Ana, et al.
  Được phát hành: (2010)
• Genome-wide Studies of Copy Number Variation and Exome Sequencing Identify Rare Variants in BAG3 as a Cause of Dilated Cardiomyopathy
  Bằng: Norton, Nadine, et al.
  Được phát hành: (2011)
• Coding sequence rare variants identified in MYBPC3, MYH6, TPM1, TNNC1 and TNNI3 from 312 patients with familial or idiopathic dilated cardiomyopathy
  Bằng: Hershberger, Ray E., et al.
  Được phát hành: (2010)