APA
Huang L., Szymanska K., Jensen V. L., Janecke A. R., Innes A. M., Davis E. E., Frosk P., Li C., Willer J. R., Chodirker B. N., Greenberg C. R., McLeod D. R., Bernier F. P., Chudley A. E., Müller T., Shboul M., Logan C. V., Loucks C. M., Beaulieu C. L., Bowie R. V., Bell S. M., Adkins J., Zuniga F. I., Ross K. D., Wang J., Ban M. R., Becker C., Nürnberg P., Douglas S., Craft C. M., Akimenko M., Hegele R. A., Ober C., Utermann G., Bolz H. J., Bulman D. E., Katsanis N., Blacque O. E., Doherty D., Parboosingh J. S., Leroux M. R., Johnson C. A. & Boycott K. M. (20120202). TMEM237 is mutated in individuals with a Joubert syndrome related disorder and expands the role of the TMEM family at the ciliary transition zone. : American journal of human genetics.
Chicago
Huang Lijia, Szymanska Katarzyna, Jensen Victor L, Janecke Andreas R, Innes A Micheil, Davis Erica E, Frosk Patrick, Li Chunmei, Willer Jason R, Chodirker Bernard N, Greenberg Cheryl R, McLeod D Ross, Bernier Francois P, Chudley Albert E, Müller Thomas, Shboul Mohammad, Logan Clare V, Loucks Catrina M, Beaulieu Chandree L, Bowie Rachel V, Bell Sandra M, Adkins Jonathan, Zuniga Freddi I, Ross Kevin D, Wang Jian, Ban Matthew R, Becker Christian, Nürnberg Peter, Douglas Stuart, Craft Cheryl M, Akimenko Marie-Andree, Hegele Robert A, Ober Carole, Utermann Gerd, Bolz Hanno J, Bulman Dennis E, Katsanis Nicholas, Blacque Oliver E, Doherty Dan, Parboosingh Jillian S, Leroux Michel R, Johnson Colin A and Boycott Kym M. 20120202. TMEM237 is mutated in individuals with a Joubert syndrome related disorder and expands the role of the TMEM family at the ciliary transition zone. : American journal of human genetics.
Harvard
Huang L., Szymanska K., Jensen V. L., Janecke A. R., Innes A. M., Davis E. E., Frosk P., Li C., Willer J. R., Chodirker B. N., Greenberg C. R., McLeod D. R., Bernier F. P., Chudley A. E., Müller T., Shboul M., Logan C. V., Loucks C. M., Beaulieu C. L., Bowie R. V., Bell S. M., Adkins J., Zuniga F. I., Ross K. D., Wang J., Ban M. R., Becker C., Nürnberg P., Douglas S., Craft C. M., Akimenko M., Hegele R. A., Ober C., Utermann G., Bolz H. J., Bulman D. E., Katsanis N., Blacque O. E., Doherty D., Parboosingh J. S., Leroux M. R., Johnson C. A. and Boycott K. M. (20120202). TMEM237 is mutated in individuals with a Joubert syndrome related disorder and expands the role of the TMEM family at the ciliary transition zone. : American journal of human genetics.
MLA
Huang Lijia, Szymanska Katarzyna, Jensen Victor L, Janecke Andreas R, Innes A Micheil, Davis Erica E, Frosk Patrick, Li Chunmei, Willer Jason R, Chodirker Bernard N, Greenberg Cheryl R, McLeod D Ross, Bernier Francois P, Chudley Albert E, Müller Thomas, Shboul Mohammad, Logan Clare V, Loucks Catrina M, Beaulieu Chandree L, Bowie Rachel V, Bell Sandra M, Adkins Jonathan, Zuniga Freddi I, Ross Kevin D, Wang Jian, Ban Matthew R, Becker Christian, Nürnberg Peter, Douglas Stuart, Craft Cheryl M, Akimenko Marie-Andree, Hegele Robert A, Ober Carole, Utermann Gerd, Bolz Hanno J, Bulman Dennis E, Katsanis Nicholas, Blacque Oliver E, Doherty Dan, Parboosingh Jillian S, Leroux Michel R, Johnson Colin A and Boycott Kym M. TMEM237 is mutated in individuals with a Joubert syndrome related disorder and expands the role of the TMEM family at the ciliary transition zone. : American journal of human genetics. 20120202.