Electron microscopy in myofibrillar myopathies reveals clues to the mutated gene-Reference-Cited by-同舟云学术

Electron microscopy in myofibrillar myopathies reveals clues to the mutated gene

Published:2008-08 Issue:8 Volume:18 Page:656-666
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Claeys K.G.,Fardeau M.,Schröder R.,Suominen T.,Tolksdorf K.,Behin A.,Dubourg O.,Eymard B.,Maisonobe T.,Stojkovic T.,Faulkner G.,Richard P.,Vicart P.,Udd B.,Voit T.,Stoltenburg G.

Publisher

Elsevier BV

Subject

Genetics(clinical),Clinical Neurology,Neurology,Pediatrics, Perinatology, and Child Health

Reference30 articles.

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3. Mutations in myotilin cause myofibrillar myopathy;Selcen;Neurology,2004

4. Mutations in ZASP define a novel form of muscular dystrophy in humans;Selcen;Ann Neurol,2005

5. A mutation in the dimerization domain of filamin c causes a novel type of autosomal dominant myofibrillar myopathy;Vorgerd;Am J Hum Genet,2005

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