X-linked fetal cardiomyopathy caused by a novel mutation in the TAZ gene

Objectives Mutations in the tafazzin (TAZ) gene at chromosomal locus Xq28 are responsible for Barth syndrome (BTHS), X‐linked endocardial fibroelastosis (EFE), X‐linked fatal infantile dilated cardiomyopathy (CMD3A), and familial isolated noncompaction of left ventricular myocardium (INVM). This eva...

Ausführliche Beschreibung

Gespeichert in:

Bibliographische Detailangaben
Veröffentlicht in:	Prenatal diagnosis 2006-05, Vol.26 (5), p.462-465
Hauptverfasser:	Brady, April N., Shehata, Bahig M., Fernhoff, Paul M.
Format:	Artikel
Sprache:	eng
Schlagworte:	Barth syndrome Biological and medical sciences Cardiology. Vascular system Cardiomyopathies - congenital Cardiomyopathies - genetics Cardiomyopathies - pathology cardiomyopathy Chromosomes, Human, X Female fetal pathology Gynecology. Andrology. Obstetrics Heart Humans Infant, Newborn Male Management. Prenatal diagnosis Medical sciences Myocarditis. Cardiomyopathies Pedigree Point Mutation Pregnancy Pregnancy. Fetus. Placenta Prenatal Diagnosis Proteins - genetics TAZ Transcription Factors - genetics
Online-Zugang:	Volltext
Tags:	Tag hinzufügen Keine Tags, Fügen Sie den ersten Tag hinzu!

Schreiben Sie den ersten Kommentar!