Single nucleotide polymorphism of NKX2-5 gene with sporadic congenital heart disease in Chinese Bai population

Congenital heart disease (CHD) is the most common birth abnormality, especially for sporadic CHD. However, the etiology of sporadic CHD is largely unknown. NKX2-5, the earliest sign of cardiac progenitor cell differentiation, plays a key role in cardiac morphogenesis, and the mutation of this gene c...

Ausführliche Beschreibung

Bibliographische Detailangaben

Veröffentlicht in:	International journal of clinical and experimental pathology 2015-01, Vol.8 (11), p.14917-14924
Hauptverfasser:	Cao, Yu, Lan, Weixing, Li, Yaxiong, Wei, Chuanyu, Zou, Honglin, Jiang, Lihong
Format:	Artikel
Sprache:	eng
Schlagworte:	Adolescent Asian People - genetics Child Female Genetic Predisposition to Disease - genetics Genotype Heart Defects, Congenital - genetics Homeobox Protein Nkx-2.5 Homeodomain Proteins - genetics Humans Male Original Polymorphism, Single Nucleotide Reverse Transcriptase Polymerase Chain Reaction Transcription Factors - genetics
Online-Zugang:	Volltext
Tags:	Tag hinzufügen Keine Tags, Fügen Sie den ersten Tag hinzu!