APA

Rohrbach M., Spencer H. L., Porter L. F., Burkitt-Wright E. M. M., Bürer C., Janecke A., Bakshi M., Sillence D., Al-Hussain H., Baumgartner M., Steinmann B., Black G. C. M., Manson F. D. C. & Giunta C. (20140122). ZNF469 frequently mutated in the brittle cornea syndrome (BCS) is a single exon gene possibly regulating the expression of several extracellular matrix components. : Molecular genetics and metabolism.

Chicago

Rohrbach Marianne, Spencer Helen L, Porter Louise F, Burkitt-Wright Emma M M, Bürer Céline, Janecke Andreas, Bakshi Madhura, Sillence David, Al-Hussain Hailah, Baumgartner Matthias, Steinmann Beat, Black Graeme C M, Manson Forbes D C and Giunta Cecilia. 20140122. ZNF469 frequently mutated in the brittle cornea syndrome (BCS) is a single exon gene possibly regulating the expression of several extracellular matrix components. : Molecular genetics and metabolism.

Harvard

Rohrbach M., Spencer H. L., Porter L. F., Burkitt-Wright E. M. M., Bürer C., Janecke A., Bakshi M., Sillence D., Al-Hussain H., Baumgartner M., Steinmann B., Black G. C. M., Manson F. D. C. and Giunta C. (20140122). ZNF469 frequently mutated in the brittle cornea syndrome (BCS) is a single exon gene possibly regulating the expression of several extracellular matrix components. : Molecular genetics and metabolism.

MLA

Rohrbach Marianne, Spencer Helen L, Porter Louise F, Burkitt-Wright Emma M M, Bürer Céline, Janecke Andreas, Bakshi Madhura, Sillence David, Al-Hussain Hailah, Baumgartner Matthias, Steinmann Beat, Black Graeme C M, Manson Forbes D C and Giunta Cecilia. ZNF469 frequently mutated in the brittle cornea syndrome (BCS) is a single exon gene possibly regulating the expression of several extracellular matrix components. : Molecular genetics and metabolism. 20140122.