The utility of copy number variation (CNV) in studies of hypertension-related left ventricular hypertrophy (LVH): Rationale, potential and challenges

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The utility of copy number variation (CNV) in studies of hypertension-related left ventricular hypertrophy (LVH): Rationale, potential and challenges

The ultimate goal of human genetics is to understand the role of genome variation in elucidating human traits and diseases. Besides single nucleotide polymorphism (SNP), copy number variation (CNV), defined as gains or losses of a DNA segment larger than 1 kb, has recently emerged as an important to...

书目详细资料
发表在:	Molecular Cytogenetics
主要作者:	Boon-Peng H.; Yusoff K.
格式:	Review
语言:	English
出版:	BioMed Central Ltd. 2013
在线阅读:	https://www.scopus.com/inward/record.uri?eid=2-s2.0-85040956304&doi=10.1186%2f1755-8166-6-8&partnerID=40&md5=5583275bb21358787182d473b93566b6

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