3 results
A presumably benign human ether-a-go-go-related gene mutation (R176W) with a malignant primary manifestation of long QT syndrome
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- Journal:
- Cardiology in the Young / Volume 22 / Issue 3 / June 2012
- Published online by Cambridge University Press:
- 09 November 2011, pp. 360-363
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Ventricular septal defect and restrictive cardiomyopathy in a paediatric TNNI3 mutation carrier
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- Journal:
- Cardiology in the Young / Volume 20 / Issue 5 / October 2010
- Published online by Cambridge University Press:
- 23 June 2010, pp. 574-576
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Cognitive/personality pattern and triplet expansion size in adult myotonic dystrophy type 1 (DM1): CTG repeats, cognition and personality in DM1
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- Journal:
- Psychological Medicine / Volume 40 / Issue 3 / March 2010
- Published online by Cambridge University Press:
- 23 July 2009, pp. 487-495
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