APA

Pedurupillay C. R. J., Amundsen S. S., Barøy T., Rasmussen M., Blomhoff A., Stadheim B. F., Ørstavik K., Holmgren A., Iqbal T., Frengen E., Misceo D. & Strømme P. (20180125). Clinical and molecular characteristics in three families with biallelic mutations in IGHMBP2. : Neuromuscular disorders : NMD.

Chicago

Pedurupillay Christeen Ramane J, Amundsen Silja S, Barøy Tuva, Rasmussen Magnhild, Blomhoff Anne, Stadheim Barbro Fossøy, Ørstavik Kristin, Holmgren Asbjørn, Iqbal Tahir, Frengen Eirik, Misceo Doriana and Strømme Petter. 20180125. Clinical and molecular characteristics in three families with biallelic mutations in IGHMBP2. : Neuromuscular disorders : NMD.

Harvard

Pedurupillay C. R. J., Amundsen S. S., Barøy T., Rasmussen M., Blomhoff A., Stadheim B. F., Ørstavik K., Holmgren A., Iqbal T., Frengen E., Misceo D. and Strømme P. (20180125). Clinical and molecular characteristics in three families with biallelic mutations in IGHMBP2. : Neuromuscular disorders : NMD.

MLA

Pedurupillay Christeen Ramane J, Amundsen Silja S, Barøy Tuva, Rasmussen Magnhild, Blomhoff Anne, Stadheim Barbro Fossøy, Ørstavik Kristin, Holmgren Asbjørn, Iqbal Tahir, Frengen Eirik, Misceo Doriana and Strømme Petter. Clinical and molecular characteristics in three families with biallelic mutations in IGHMBP2. : Neuromuscular disorders : NMD. 20180125.