MBNL1 gene variants as modifiers of disease severity in myotonic dystrophy type 1-Reference-Cited by-同舟云学术

MBNL1 gene variants as modifiers of disease severity in myotonic dystrophy type 1

Published:2012-11-16 Issue:4 Volume:260 Page:998-1003
ISSN:0340-5354
Container-title:Journal of Neurology
language:en
Short-container-title:J Neurol

Author:

Huin Vincent,Vasseur Francis,Schraen-Maschke Susanna,Dhaenens Claire-Marie,Devos Patrick,Dupont Kathy,Sergeant Nicolas,Buée Luc,Lacour Arnaud,Hofmann-Radvanyi Hélène,Sablonnière Bernard

Publisher

Springer Science and Business Media LLC

Subject

Neurology (clinical),Neurology

Link

http://link.springer.com/content/pdf/10.1007/s00415-012-6740-y.pdf

Reference27 articles.

1. Harper PS (2001) Myotonic dystrophy. In: 3rd edn. WB Saunders, London

2. Brook JD, Mc Currach ME, Harley HG et al (1992) Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3′ end of a transcript encoding a protein kinase family member. Cell 68(4):799–808

3. Harper PS (2004) Myotonic dystrophy: present management, future therapy. Oxford University Press, Oxford

4. Turner C, Hilton-Jones D (2010) The myotonic dystrophies: diagnosis and management. J Neurol Neurosurg Psychiatry 81:358–367

5. Arsenault ME, Prevost C, Lescault A et al (2006) Clinical characteristics of myotonic dystrophy type 1 patients with small CTG expansions. Neurology 66(8):1248–1250

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