ISPD gene mutations are a common cause of congenital and limb-girdle muscular dystrophies.
Cirak S; Foley AR; Herrmann R; Willer T; Yau S; Stevens E; Torelli S; Brodd L; Kamynina A; Vondracek P; Roper H; Longman C; Korinthenberg R; Marrosu G; Nürnberg P; Michele DE; Plagnol V; Hurles M; Moore SA; Sewry CA; Campbell KP; Voit T; Muntoni F; Brain: A Journal Of Neurology, 2013, vol. 136, issue Pt 1, p 269, ISSN 14602156. ISBN 14602156.

Full Text Resources Located for this Citation

View article on EBSCOhost(Login required)
View article via CrossRef