APA

Sergouniotis P. I., Chakarova C., Murphy C., Becker M., Lenassi E., Arno G., Lek M., MacArthur D. G., Bhattacharya S. S., Moore A. T., Holder G. E., Robson A. G., Wolfrum U., Webster A. R. & Plagnol V. (20140627). Biallelic variants in TTLL5, encoding a tubulin glutamylase, cause retinal dystrophy. : American journal of human genetics.

Chicago

Sergouniotis Panagiotis I, Chakarova Christina, Murphy Cian, Becker Mirjana, Lenassi Eva, Arno Gavin, Lek Monkol, MacArthur Daniel G, Bhattacharya Shomi S, Moore Anthony T, Holder Graham E, Robson Anthony G, Wolfrum Uwe, Webster Andrew R and Plagnol Vincent. 20140627. Biallelic variants in TTLL5, encoding a tubulin glutamylase, cause retinal dystrophy. : American journal of human genetics.

Harvard

Sergouniotis P. I., Chakarova C., Murphy C., Becker M., Lenassi E., Arno G., Lek M., MacArthur D. G., Bhattacharya S. S., Moore A. T., Holder G. E., Robson A. G., Wolfrum U., Webster A. R. and Plagnol V. (20140627). Biallelic variants in TTLL5, encoding a tubulin glutamylase, cause retinal dystrophy. : American journal of human genetics.

MLA

Sergouniotis Panagiotis I, Chakarova Christina, Murphy Cian, Becker Mirjana, Lenassi Eva, Arno Gavin, Lek Monkol, MacArthur Daniel G, Bhattacharya Shomi S, Moore Anthony T, Holder Graham E, Robson Anthony G, Wolfrum Uwe, Webster Andrew R and Plagnol Vincent. Biallelic variants in TTLL5, encoding a tubulin glutamylase, cause retinal dystrophy. : American journal of human genetics. 20140627.