Female and Male Carriers of TAZ Mutations Need to be Thoroughly Investigated
- PMID: 29876239
- PMCID: PMC5972509
- DOI: 10.1515/bjmg-2017-0030
Female and Male Carriers of TAZ Mutations Need to be Thoroughly Investigated
References
-
- Spencer CT, Bryant RM, Day J, Gonzalez IL, Colan SD, Thompson WR. et al. Cardiac and clinical phenotype in Barth syndrome. Pediatrics. 2006;118(2):e337–46. - PubMed
-
- Burke A, Mont E, Kutys R, Virmani R.. Left ventricular noncompaction: a pathological study of 14 cases. Hum Pathol. 2005;36(4):403–411. - PubMed
-
- Woiewodski L, Ezon D, Cooper J, Feingold B.. Barth Syndrome with late-onset cardiomyopathy: A missed opportunity for diagnosis. J Pediatr. 2017;183:196–198. - PubMed
-
- Stollberger C, Wegner C, Finsterer J.. Fetal ventricular hypertrabeculation/noncompaction: Clinical presentation, genetics, associated cardiac and extracardiac abnormalities and outcome. Pediatr Cardiol. 2015;36(7):1319–1326. - PubMed
LinkOut - more resources
Full Text Sources
Other Literature Sources