Identification of mutations in theMYO9Agene in patients with congenital myasthenic syndrome-Reference-Cited by-同舟云学术

Identification of mutations in theMYO9Agene in patients with congenital myasthenic syndrome

Published:2016-06-03 Issue:8 Volume:139 Page:2143-2153
ISSN:0006-8950
Container-title:Brain
language:en
Short-container-title:Brain

Author:

O’Connor Emily,Töpf Ana,Müller Juliane S.,Cox Daniel,Evangelista Teresinha,Colomer Jaume,Abicht Angela,Senderek Jan,Hasselmann Oswald,Yaramis Ahmet,Laval Steven H.,Lochmüller Hanns

Publisher

Oxford University Press (OUP)

Subject

Neurology (clinical)

Link

http://academic.oup.com/brain/article-pdf/139/8/2143/17944623/aww130.pdf

Reference47 articles.

1. Myosin IXa Regulates Epithelial Differentiation and Its Deficiency Results in Hydrocephalus

2. Zebrafish models of human motor neuron diseases: Advantages and limitations

3. Molecular etiology of arthrogryposis in multiple families of mostly Turkish origin

4. Identification ofDPAGT1as a new gene in which mutations cause a congenital myasthenic syndrome

5. Mutations inGMPPBcause congenital myasthenic syndrome and bridge myasthenic disorders with dystroglycanopathies

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