Dystroglycan and Dystroglycanopathies: Report of the 187th ENMC Workshop 11-13 November 2011, Naarden, The Netherlands

Overview

Journal Neuromuscul Disord

Specialty Neurology

Date 2012 Mar 23

PMID 22437172

Citations 4

Authors

Susan C Brown

Steve J Winder

Affiliations

Soon will be listed here.

Citing Articles

FKRP-dependent glycosylation of fibronectin regulates muscle pathology in muscular dystrophy.

Wood A, Lin C, Li M, Nishtala K, Alaei S, Rossello F Nat Commun. 2021; 12(1):2951.

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ISPD mutations account for a small proportion of Italian Limb Girdle Muscular Dystrophy cases.

Magri F, Colombo I, Del Bo R, Previtali S, Brusa R, Ciscato P BMC Neurol. 2015; 15:172.

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Neuromuscular disorders in zebrafish: state of the art and future perspectives.

Pappalardo A, Pitto L, Fiorillo C, Donati M, Bruno C, Santorelli F Neuromolecular Med. 2013; 15(2):405-19.

PMID: 23584918 DOI: 10.1007/s12017-013-8228-z.

ISPD gene mutations are a common cause of congenital and limb-girdle muscular dystrophies.

Cirak S, Foley A, Herrmann R, Willer T, Yau S, Stevens E Brain. 2013; 136(Pt 1):269-81.

PMID: 23288328 PMC: 3562076. DOI: 10.1093/brain/aws312.

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