Human Genetics of Truncus Arteriosus View Full Text


Ontology type: schema:Chapter     


Chapter Info

DATE

2016

AUTHORS

Hiroyuki Yamagishi

ABSTRACT

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.

PAGES

559-567

Book

TITLE

Congenital Heart Diseases: The Broken Heart

ISBN

978-3-7091-1882-5
978-3-7091-1883-2

Author Affiliations

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/978-3-7091-1883-2_47

DOI

http://dx.doi.org/10.1007/978-3-7091-1883-2_47

DIMENSIONS

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