Human genetics of truncus arteriosus

Hiroyuki Yamagishi

doi:10.1007/978-3-7091-1883-2_47

Human genetics of truncus arteriosus

Hiroyuki Yamagishi

小児科学

研究成果: Chapter

1 被引用数 (Scopus)

抄録

Human genetic studies have revealed that truncus arteriosus is highly associated with 22q11.2 deletion syndrome. Other congenital malformation syndromes and mutations in genes encoding NKX and GATA transcription factors have also been reported as its etiology.

本文言語	English
ホスト出版物のタイトル	Congenital Heart Diseases: The Broken Heart: Clinical Features, Human Genetics and Molecular Pathways
出版社	Springer-Verlag Wien
ページ	559-568
ページ数	10
ISBN（電子版）	9783709118832
ISBN（印刷版）	9783709118825
DOI	https://doi.org/10.1007/978-3-7091-1883-2_47
出版ステータス	Published - 2015 1 1

ASJC Scopus subject areas

Biochemistry, Genetics and Molecular Biology(all)
Medicine(all)

文献へのアクセス

10.1007/978-3-7091-1883-2_47

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引用スタイル

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