APA
Zazo Seco C., Castells-Nobau A., Joo S., Schraders M., Foo J. N., van der Voet M., Velan S. S., Nijhof B., Oostrik J., de Vrieze E., Katana R., Mansoor A., Huynen M., Szklarczyk R., Oti M., Tranebjærg L., van Wijk E., Scheffer-de Gooyert J. M., Siddique S., Baets J., de Jonghe P., Kazmi S. A. R., Sadananthan S. A., van de Warrenburg B. P., Khor C. C., Göpfert M. C., Qamar R., Schenck A., Kremer H. & Siddiqi S. (20171204). A homozygous FITM2 mutation causes a deafness-dystonia syndrome with motor regression and signs of ichthyosis and sensory neuropathy. : Disease models & mechanisms.
Chicago
Zazo Seco Celia, Castells-Nobau Anna, Joo Seol-Hee, Schraders Margit, Foo Jia Nee, van der Voet Monique, Velan S Sendhil, Nijhof Bonnie, Oostrik Jaap, de Vrieze Erik, Katana Radoslaw, Mansoor Atika, Huynen Martijn, Szklarczyk Radek, Oti Martin, Tranebjærg Lisbeth, van Wijk Erwin, Scheffer-de Gooyert Jolanda M, Siddique Saadat, Baets Jonathan, de Jonghe Peter, Kazmi Syed Ali Raza, Sadananthan Suresh Anand, van de Warrenburg Bart P, Khor Chiea Chuen, Göpfert Martin C, Qamar Raheel, Schenck Annette, Kremer Hannie and Siddiqi Saima. 20171204. A homozygous FITM2 mutation causes a deafness-dystonia syndrome with motor regression and signs of ichthyosis and sensory neuropathy. : Disease models & mechanisms.
Harvard
Zazo Seco C., Castells-Nobau A., Joo S., Schraders M., Foo J. N., van der Voet M., Velan S. S., Nijhof B., Oostrik J., de Vrieze E., Katana R., Mansoor A., Huynen M., Szklarczyk R., Oti M., Tranebjærg L., van Wijk E., Scheffer-de Gooyert J. M., Siddique S., Baets J., de Jonghe P., Kazmi S. A. R., Sadananthan S. A., van de Warrenburg B. P., Khor C. C., Göpfert M. C., Qamar R., Schenck A., Kremer H. and Siddiqi S. (20171204). A homozygous FITM2 mutation causes a deafness-dystonia syndrome with motor regression and signs of ichthyosis and sensory neuropathy. : Disease models & mechanisms.
MLA
Zazo Seco Celia, Castells-Nobau Anna, Joo Seol-Hee, Schraders Margit, Foo Jia Nee, van der Voet Monique, Velan S Sendhil, Nijhof Bonnie, Oostrik Jaap, de Vrieze Erik, Katana Radoslaw, Mansoor Atika, Huynen Martijn, Szklarczyk Radek, Oti Martin, Tranebjærg Lisbeth, van Wijk Erwin, Scheffer-de Gooyert Jolanda M, Siddique Saadat, Baets Jonathan, de Jonghe Peter, Kazmi Syed Ali Raza, Sadananthan Suresh Anand, van de Warrenburg Bart P, Khor Chiea Chuen, Göpfert Martin C, Qamar Raheel, Schenck Annette, Kremer Hannie and Siddiqi Saima. A homozygous FITM2 mutation causes a deafness-dystonia syndrome with motor regression and signs of ichthyosis and sensory neuropathy. : Disease models & mechanisms. 20171204.