Familial Atrial Septal Defect and Sudden Cardiac Death: Identification of a Novel NKX2-5 Mutation and a Review of the Literature.
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Mutation of a common amino acid in NKX2.5 results in dilated cardiomyopathy in two large families.An update on the molecular diagnosis of congenital heart disease: focus on loss-of-function mutations.MEF2C loss-of-function mutation contributes to congenital heart defects.Nkx2-3-A Slippery Slope From Development Through Inflammation Toward Hematopoietic Malignancies.Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes.Arrhythmias and conduction disorders associated with atrial septal defectsElectrical disorders in atrial septal defect: genetics and heritability
P2860
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P2860
Familial Atrial Septal Defect and Sudden Cardiac Death: Identification of a Novel NKX2-5 Mutation and a Review of the Literature.
description
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 18 December 2015
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vedecký článok
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vetenskaplig artikel
@sv
videnskabelig artikel
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vědecký článek
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name
Familial Atrial Septal Defect ...... nd a Review of the Literature.
@en
Familial Atrial Septal Defect ...... nd a Review of the Literature.
@nl
type
label
Familial Atrial Septal Defect ...... nd a Review of the Literature.
@en
Familial Atrial Septal Defect ...... nd a Review of the Literature.
@nl
prefLabel
Familial Atrial Septal Defect ...... nd a Review of the Literature.
@en
Familial Atrial Septal Defect ...... nd a Review of the Literature.
@nl
P2093
P2860
P50
P921
P356
P1476
Familial Atrial Septal Defect ...... nd a Review of the Literature.
@en
P2093
Jesper Vandborg Bjerre
Morten Munk Johansen
Sabrina Gade Ellesøe
P2860
P304
P356
10.1111/CHD.12317
P5008
P577
2015-12-18T00:00:00Z
2016-05-01T00:00:00Z