Combined cardiological and neurological abnormalities due to filamin A gene mutation-Reference-Cited by-同舟云学术

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Combined cardiological and neurological abnormalities due to filamin A gene mutation

Published:2010-08-22 Issue:1 Volume:100 Page:45-50
ISSN:1861-0684
Container-title:Clinical Research in Cardiology
language:en
Short-container-title:Clin Res Cardiol

Author:

de Wit Marie Claire Y.,de Coo Irenaeus F. M.,Lequin Maarten H.,Halley Dicky J. J.,Roos-Hesselink Jolien W.,Mancini Grazia M. S.

Publisher

Springer Science and Business Media LLC

Subject

Cardiology and Cardiovascular Medicine,General Medicine

Link

http://link.springer.com/content/pdf/10.1007/s00392-010-0206-y

Reference23 articles.

1. König K, Will JC, Berger F, Müller D, Benson DW (2006) Familial congenital heart disease, progressive atrioventricular block and the cardiac homeobox transcription factor gene NKX2.5: identification of a novel mutation. Clin Res Cardiol 95(9):499–503

2. Posch MG, Perrot A, Berger F, Ozcelik C (2010) Molecular genetics of congenital atrial septal defects. Clin Res Cardiol 99(3):137–147

3. Lauschke J, Maisch B (2009) Athlete’s heart or hypertrophic cardiomyopathy? Clin Res Cardiol 98(2):80–88

4. Sheen VL, Dixon PH, Fox JW, Hong SE, Kinton L, Sisodiya SM, Duncan JS, Dubeau F, Scheffer IE, Schachter SC, Wilner A, Henchy R, Crino P, Kamuro K, DiMario F, Berg M, Kuzniecky R, Cole AJ, Bromfield E, Biber M, Schomer D, Wheless J, Silver K, Mochida GH, Berkovic SF, Andermann F, Andermann E, Dobyns WB, Wood NW, Walsh CA (2001) Mutations in the X-linked filamin 1 gene cause periventricular nodular heterotopia in males as well as in females. Hum Mol Genet 10(17):1775–1783

5. Zhou AX, Hartwig JH, Akyürek LM (2010) Filamins in cell signaling, transcription and organ development. Trends Cell Biol 20(2):113–123

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