Phenotype of matrin-3-related distal myopathy in 16 German patients-Reference-Cited by-同舟云学术

Phenotype of matrin-3-related distal myopathy in 16 German patients

Published:2014-09-16 Issue:5 Volume:76 Page:669-680
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Müller Tobias J.¹,Kraya Torsten¹,Stoltenburg-Didinger Gisela¹²,Hanisch Frank¹,Kornhuber Malte¹,Stoevesandt Dietrich³,Senderek Jan⁴,Weis Joachim⁵,Baum Petra⁶,Deschauer Marcus¹,Zierz Stephan¹

Affiliation:

1. Department of Neurology; Martin Luther University of Halle-Wittenberg; Halle Germany

2. Institute of Cell and Neurobiology; Charité University Medicine Berlin; Berlin Germany

3. Department of Diagnostic Radiology; Martin Luther University of Halle-Wittenberg; Halle Germany

4. Friedrich Bauer Institute; Ludwig Maximilian University of Munich; Munich Germany

5. Institute of Neuropathology; RWTH Aachen University Hospital; Aachen Germany

6. Clinic and Polyclinic for Neurology; University of Leipzig; Leipzig Germany

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference22 articles.

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2. Autosomal-dominant distal myopathy associated with a recurrent missense mutation in the gene encoding the nuclear matrix protein, matrin 3;Senderek;Am J Hum Genet,2009

3. Maintenance of a functional higher order chromatin structure: the role of the nuclear matrix in normal and disease states;Linnemann;Gene Ther Mol Biol,2009

4. Functions of the nuclear envelope and lamina in development and disease;Cohen;Biochem Soc Trans,2008

5. Matrin 3: chromosomal distribution and protein interactions;Zeitz;J Cell Biochem,2009

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