APA
Farazi Fard M. A., Rebelo A. P., Buglo E., Nemati H., Dastsooz H., Gehweiler I., Reich S., Reichbauer J., Quintáns B., Ordóñez-Ugalde A., Cortese A., Courel S., Abreu L., Powell E., Danzi M. C., Martuscelli N. B., Bis-Brewer D. M., Tao F., Zarei F., Habibzadeh P., Yavarian M., Modarresi F., Silawi M., Tabatabaei Z., Yousefi M., Farpour H. R., Kessler C., Mangold E., Kobeleva X., Tournev I., Chamova T., Mueller A. J., Haack T. B., Tarnopolsky M., Gan-Or Z., Rouleau G. A., Synofzik M., Sobrido M., Jordanova A., Schüle R., Zuchner S. & Faghihi M. A. (2019). Truncating Mutations in UBAP1 Cause Hereditary Spastic Paraplegia. : American journal of human genetics.
Chicago
Farazi Fard Mohammad Ali, Rebelo Adriana P, Buglo Elena, Nemati Hamid, Dastsooz Hassan, Gehweiler Ina, Reich Selina, Reichbauer Jennifer, Quintáns Beatriz, Ordóñez-Ugalde Andrés, Cortese Andrea, Courel Steve, Abreu Lisa, Powell Eric, Danzi Matt C, Martuscelli Nicole B, Bis-Brewer Dana M, Tao Feifei, Zarei Fariba, Habibzadeh Parham, Yavarian Majid, Modarresi Farzaneh, Silawi Mohammad, Tabatabaei Zahra, Yousefi Masoume, Farpour Hamid Reza, Kessler Christoph, Mangold Elisabeth, Kobeleva Xenia, Tournev Ivailo, Chamova Teodora, Mueller Amelie J, Haack Tobias B, Tarnopolsky Mark, Gan-Or Ziv, Rouleau Guy A, Synofzik Matthis, Sobrido María-Jesús, Jordanova Albena, Schüle Rebecca, Zuchner Stephan and Faghihi Mohammad Ali. 2019. Truncating Mutations in UBAP1 Cause Hereditary Spastic Paraplegia. : American journal of human genetics.
Harvard
Farazi Fard M. A., Rebelo A. P., Buglo E., Nemati H., Dastsooz H., Gehweiler I., Reich S., Reichbauer J., Quintáns B., Ordóñez-Ugalde A., Cortese A., Courel S., Abreu L., Powell E., Danzi M. C., Martuscelli N. B., Bis-Brewer D. M., Tao F., Zarei F., Habibzadeh P., Yavarian M., Modarresi F., Silawi M., Tabatabaei Z., Yousefi M., Farpour H. R., Kessler C., Mangold E., Kobeleva X., Tournev I., Chamova T., Mueller A. J., Haack T. B., Tarnopolsky M., Gan-Or Z., Rouleau G. A., Synofzik M., Sobrido M., Jordanova A., Schüle R., Zuchner S. and Faghihi M. A. (2019). Truncating Mutations in UBAP1 Cause Hereditary Spastic Paraplegia. : American journal of human genetics.
MLA
Farazi Fard Mohammad Ali, Rebelo Adriana P, Buglo Elena, Nemati Hamid, Dastsooz Hassan, Gehweiler Ina, Reich Selina, Reichbauer Jennifer, Quintáns Beatriz, Ordóñez-Ugalde Andrés, Cortese Andrea, Courel Steve, Abreu Lisa, Powell Eric, Danzi Matt C, Martuscelli Nicole B, Bis-Brewer Dana M, Tao Feifei, Zarei Fariba, Habibzadeh Parham, Yavarian Majid, Modarresi Farzaneh, Silawi Mohammad, Tabatabaei Zahra, Yousefi Masoume, Farpour Hamid Reza, Kessler Christoph, Mangold Elisabeth, Kobeleva Xenia, Tournev Ivailo, Chamova Teodora, Mueller Amelie J, Haack Tobias B, Tarnopolsky Mark, Gan-Or Ziv, Rouleau Guy A, Synofzik Matthis, Sobrido María-Jesús, Jordanova Albena, Schüle Rebecca, Zuchner Stephan and Faghihi Mohammad Ali. Truncating Mutations in UBAP1 Cause Hereditary Spastic Paraplegia. : American journal of human genetics. 2019.