Mutations in the NOTCH pathway regulator MIB1 cause left ventricular noncompaction cardiomyopathy-Reference-Cited by-同舟云学术

Mutations in the NOTCH pathway regulator MIB1 cause left ventricular noncompaction cardiomyopathy

Published:2013-01-13 Issue:2 Volume:19 Page:193-201
ISSN:1078-8956
Container-title:Nature Medicine
language:en
Short-container-title:Nat Med

Author:

Luxán Guillermo,Casanova Jesús C,Martínez-Poveda Beatriz,Prados Belén,D'Amato Gaetano,MacGrogan Donal,Gonzalez-Rajal Alvaro,Dobarro David,Torroja Carlos,Martinez Fernando,Izquierdo-García José Luis,Fernández-Friera Leticia,Sabater-Molina María,Kong Young-Y,Pizarro Gonzalo,Ibañez Borja,Medrano Constancio,García-Pavía Pablo,Gimeno Juan R,Monserrat Lorenzo,Jiménez-Borreguero Luis J,de la Pompa José Luis

Publisher

Springer Science and Business Media LLC

Subject

General Biochemistry, Genetics and Molecular Biology,General Medicine

Link

http://www.nature.com/articles/nm.3046.pdf

Reference83 articles.

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2. Sedmera, D., Pexieder, T., Vuillemin, M., Thompson, R.P. & Anderson, R.H. Developmental patterning of the myocardium. Anat. Rec. 258, 319–337 (2000).

3. Towbin, J.A. Left ventricular noncompaction: a new form of heart failure. Heart Fail. Clin. 6, 453–469, viii (2010).

4. Captur, G. & Nihoyannopoulos, P. Left ventricular non-compaction: genetic heterogeneity, diagnosis and clinical course. Int. J. Cardiol. 140, 145–153 (2010).

5. Oechslin, E.N., Attenhofer Jost, C.H., Rojas, J.R., Kaufmann, P.A. & Jenni, R. Long-term follow-up of 34 adults with isolated left ventricular noncompaction: a distinct cardiomyopathy with poor prognosis. J. Am. Coll. Cardiol. 36, 493–500 (2000).

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