Mutation in ST6GALNAC5 identified in family with coronary artery disease.
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Genetics of coronary artery disease and myocardial infarctionmiRNA proxy approach reveals hidden functions of glycosylationSequences of 95 human MHC haplotypes reveal extreme coding variation in genes other than highly polymorphic HLA class I and II.Epigenome-wide association study reveals differential DNA methylation in individuals with a history of myocardial infarction.
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Mutation in ST6GALNAC5 identified in family with coronary artery disease.
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article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on 08 January 2014
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Mutation in ST6GALNAC5 identified in family with coronary artery disease.
@en
Mutation in ST6GALNAC5 identified in family with coronary artery disease.
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type
label
Mutation in ST6GALNAC5 identified in family with coronary artery disease.
@en
Mutation in ST6GALNAC5 identified in family with coronary artery disease.
@nl
prefLabel
Mutation in ST6GALNAC5 identified in family with coronary artery disease.
@en
Mutation in ST6GALNAC5 identified in family with coronary artery disease.
@nl
P2093
P2860
P356
P1433
P1476
Mutation in ST6GALNAC5 identified in family with coronary artery disease.
@en
P2093
Amir Farhang Zand Parsa
Casey Turk
Elahe Elahi
Frank Steemers
Jian-Bing Fan
Kevin Gunderson
Kolsoum InanlooRahatloo
Marcel Kramer
Mostafa Ronaghi
Paniz Rasooli
P2860
P2888
P356
10.1038/SREP03595
P407
P577
2014-01-08T00:00:00Z