Diagnosis and etiology of congenital muscular dystrophy: We are halfway there.

Authors

Gina L O'Grady
Monkol Lek
Shireen R Lamande
Leigh Waddell
Emily C Oates
Jaya Punetha, George Washington University - School of Medicine and Health Sciences
Roula Ghaoui
Sarah A Sandaradura
Heather Best
Simranpreet Kaur
Mark Davis
Nigel G Laing
Francesco Muntoni
Eric HoffmanFollow
Daniel G MacArthur
Nigel F Clarke
Sandra Cooper
Kathryn North

Document Type

Journal Article

Publication Date

7-1-2016

Student Program

IBS

Journal

Annals of Neurology

Volume

80

Issue

1

Inclusive Pages

101-111

DOI

10.1002/ana.24687

Keywords

Adolescent; Adult; Child; Child, Preschool; Collagen Type VI; Dystroglycans; Genetic Predisposition to Disease; Genetic Variation; High-Throughput Nucleotide Sequencing; Humans; Infant; Laminin; Muscle, Skeletal; Muscular Dystrophies; Young Adult

APA Citation

O'Grady, G., Lek, M., Lamande, S., Waddell, L., Oates, E., Punetha, J., Ghaoui, R., Sandaradura, S., Best, H., Kaur, S., Davis, M., Laing, N., Muntoni, F., Hoffman, E., MacArthur, D., Clarke, N., Cooper, S., & North, K. (2016). Diagnosis and etiology of congenital muscular dystrophy: We are halfway there.. Annals of Neurology, 80 (1). http://dx.doi.org/10.1002/ana.24687

Peer Reviewed

1