APA

Strang-Karlsson S., Johnson K., Töpf A., Xu L., Lek M., MacArthur D. G., Casar-Borota O., Williams M., Straub V. & Wallgren-Pettersson C. (20191022). A novel compound heterozygous mutation in the POMK gene causing limb-girdle muscular dystrophy-dystroglycanopathy in a sib pair. : Neuromuscular disorders : NMD.

Chicago

Strang-Karlsson Sonja, Johnson Katherine, Töpf Ana, Xu Liwen, Lek Monkol, MacArthur Daniel G, Casar-Borota Olivera, Williams Maria, Straub Volker and Wallgren-Pettersson Carina. 20191022. A novel compound heterozygous mutation in the POMK gene causing limb-girdle muscular dystrophy-dystroglycanopathy in a sib pair. : Neuromuscular disorders : NMD.

Harvard

Strang-Karlsson S., Johnson K., Töpf A., Xu L., Lek M., MacArthur D. G., Casar-Borota O., Williams M., Straub V. and Wallgren-Pettersson C. (20191022). A novel compound heterozygous mutation in the POMK gene causing limb-girdle muscular dystrophy-dystroglycanopathy in a sib pair. : Neuromuscular disorders : NMD.

MLA

Strang-Karlsson Sonja, Johnson Katherine, Töpf Ana, Xu Liwen, Lek Monkol, MacArthur Daniel G, Casar-Borota Olivera, Williams Maria, Straub Volker and Wallgren-Pettersson Carina. A novel compound heterozygous mutation in the POMK gene causing limb-girdle muscular dystrophy-dystroglycanopathy in a sib pair. : Neuromuscular disorders : NMD. 20191022.