Rare and low-frequency variants in human common diseases and other complex traits.
about
Application of computational methods in genetic study of inflammatory bowel diseaseFunctional genetic variants within the SIRT2 gene promoter in acute myocardial infarction.Analysis of Low Frequency Protein Truncating Stop-Codon Variants and Fasting Concentration of Growth HormoneAssessing the Power of Exome Chips.Otosclerosis Associated with a De Novo Mutation -832G > A in the TGFB1 Gene Promoter Causing a Decreased Expression Level.Estimating the mutational load for cardiovascular diseases in Pakistani population.
P2860
Rare and low-frequency variants in human common diseases and other complex traits.
description
2014 nî lūn-bûn
@nan
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
2014年论文
@zh
2014年论文
@zh-cn
name
Rare and low-frequency variants in human common diseases and other complex traits.
@en
type
label
Rare and low-frequency variants in human common diseases and other complex traits.
@en
prefLabel
Rare and low-frequency variants in human common diseases and other complex traits.
@en
P2860
P1476
Rare and low-frequency variants in human common diseases and other complex traits.
@en
P2093
Guillaume Lettre
P2860
P304
P356
10.1136/JMEDGENET-2014-102437
P407
P577
2014-09-03T00:00:00Z