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 |
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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 | |
出版ステータス | Published - 2015 1月 1 |
ASJC Scopus subject areas
- 生化学、遺伝学、分子生物学(全般)
- 医学(全般)