DNAH11 variants and its association with congenital heart disease and heterotaxy syndrome
Author:
Publisher
Springer Science and Business Media LLC
Subject
Multidisciplinary
Link
http://www.nature.com/articles/s41598-019-43109-6.pdf
Reference21 articles.
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2. Deng, H., Xia, H. & Deng, S. Genetic basis of human left-right asymmetry disorders. Expert Rev Mol Med 16, e19, https://doi.org/10.1017/erm.2014.22 (2015).
3. Lin, A. E., Ticho, B. S., Houde, K., Westgate, M. N. & Holmes, L. B. Heterotaxy: associated conditions and hospital-based prevalence in newborns. Genet Med 2, 157–172, https://doi.org/10.1097/00125817-200005000-00002 (2000).
4. Nakhleh, N. et al. High prevalence of respiratory ciliary dysfunction in congenital heart disease patients with heterotaxy. Circulation 125, 2232–2242, https://doi.org/10.1161/CIRCULATIONAHA.111.079780 (2012).
5. Harrison, M. J., Shapiro, A. J. & Kennedy, M. P. Congenital Heart Disease and Primary CiliaryDyskinesia. PaediatrRespirRev 18, 25–32, https://doi.org/10.1016/j.prrv.2015.09.003 (2016).
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