Brain involvement in muscular dystrophies with defective dystroglycan glycosylation-Reference-Cited by-同舟云学术

Brain involvement in muscular dystrophies with defective dystroglycan glycosylation

Published:2008-11 Issue:5 Volume:64 Page:573-582
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Clement Emma,Mercuri Eugenio,Godfrey Caroline,Smith Janine,Robb Stephanie,Kinali Maria,Straub Volker,Bushby Kate,Manzur Adnan,Talim Beril,Cowan Frances,Quinlivan Ros,Klein Andrea,Longman Cheryl,McWilliam Robert,Topaloglu Haluk,Mein Rachael,Abbs Stephen,North Kathryn,Barkovich A. James,Rutherford Mary,Muntoni Francesco

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Reference58 articles.

1. Fukutin and alpha-dystroglycanopathies;Toda;Acta Myol,2005

2. Defective glycosylation in congenital muscular dystrophies;Muntoni;Curr Opin Neurol,2004

3. The congenital muscular dystrophies in 2004: a century of exciting progress;Muntoni;Neuromuscul Disord,2004

4. An autosomal recessive limb girdle muscular dystrophy (LGMD2) with mild mental retardation is allelic to Walker-Warburg syndrome (WWS) caused by a mutation in the POMT1 gene;Balci;Neuromuscul Disord,2005

5. Fukutin gene mutations in steroid-responsive limb girdle muscular dystrophy;Godfrey;Ann Neurol,2006

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