Hereditary neuralgic amyotrophy in childhood caused by duplication within the SEPT9 gene: A family study-Reference-Cited by-同舟云学术

Hereditary neuralgic amyotrophy in childhood caused by duplication within the SEPT9 gene: A family study

Published:2018-10-10 Issue:1 Volume:76 Page:131-136
ISSN:1949-3584
Container-title:Cytoskeleton
language:en
Short-container-title:Cytoskeleton

Author:

Neubauer Katharina¹,Boeckelmann Doris¹,Koehler Udo²,Kracht Julia³,Kirschner Janbernd⁴,Pendziwiat Manuela⁵,Zieger Barbara¹

Affiliation:

1. Division of Pediatric Hematology and Oncology, Department of Pediatrics and Adolescent Medicine; University Medical Center, Medical Faculty, University of Freiburg; Freiburg Germany

2. Department of Medical Genetics; MGZ - Medical Genetics Center; Munich Germany

3. Division of General Pediatrics, Department of Pediatrics and Adolescent Medicine; University Medical Center, Medical Faculty, University of Freiburg; Freiburg Germany

4. Department of Neuropediatrics and Muscle Disorders; University Medical Center, Faculty of Medicine, University of Freiburg; Germany

5. Department of Neuropediatrics; Christian-Albrechts-University of Kiel and University Medical Center Schleswig-Holstein; Kiel Germany

Funder

Deutsche Forschungsgemeinschaft

Publisher

Wiley

Subject

Cell Biology,Structural Biology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/cm.21479/fullpdf

Reference47 articles.

1. Hereditary recurrent brachial plexus neuropathy with dysmorphic features;Airaksinen;Acta Neurologica Scandinavica,1985

2. Neuralgic amyotrophy in children;Al-Ghamdi;Muscle & Nerve,2018

3. Deletion of human GP1BB and SEPT5 is associated with Bernard-Soulier syndrome, platelet secretion defect, polymicrogyria, and developmental delay;Bartsch;Thrombosis and Haemostasis,2011

4. Brachial plexus neuropathy in the population of Rochester, Minnesota, 1970-1981;Beghi;Annals of Neurology,1985

5. Bilateral neuralgic amyotrophy induced by interferon treatment;Bernsen;Archives of Neurology,1988

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