Next generation sequencing in a large cohort of patients presenting with neuromuscular disease before or at birth

Todd EJ., Yau KS., Ong R., Slee J., McGillivray G., Barnett CP., Haliloglu G., Talim B., Akcoren Z., Kariminejad A., Cairns A., Clarke NF., Freckmann M-L., Romero NB., Williams D., Sewry CA., Colley A., Ryan MM., Kiraly-Borri C., Sivadorai P., Allcock RJN., Beeson D., Maxwell S., Davis MR., Laing NG., Ravenscroft G.

DOI

10.1186/s13023-015-0364-0

Type

Journal article

Journal

Orphanet Journal of Rare Diseases

Publisher

Springer Science and Business Media LLC

Publication Date

12/2015

Volume

10

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