APA
Nemethova M., Radvanszky J., Kadasi L., Ascher D. B., Pires D. E. V., Blundell T. L., Porfirio B., Mannoni A., Santucci A., Milucci L., Sestini S., Biolcati G., Sorge F., Aurizi C., Aquaron R., Alsbou M., Lourenço C. M., Ramadevi K., Ranganath L. R., Gallagher J. A., van Kan C., Hall A. K., Olsson B., Sireau N., Ayoob H., Timmis O. G., Sang K. L. Q., Genovese F., Imrich R., Rovensky J., Srinivasaraghavan R., Bharadwaj S. K., Spiegel R. & Zatkova A. (20160919). Twelve novel HGD gene variants identified in 99 alkaptonuria patients: focus on 'black bone disease' in Italy. : European journal of human genetics : EJHG.
Chicago
Nemethova Martina, Radvanszky Jan, Kadasi Ludevit, Ascher David B, Pires Douglas E V, Blundell Tom L, Porfirio Berardino, Mannoni Alessandro, Santucci Annalisa, Milucci Lia, Sestini Silvia, Biolcati Gianfranco, Sorge Fiammetta, Aurizi Caterina, Aquaron Robert, Alsbou Mohammed, Lourenço Charles Marques, Ramadevi Kanakasabapathi, Ranganath Lakshminarayan R, Gallagher James A, van Kan Christa, Hall Anthony K, Olsson Birgitta, Sireau Nicolas, Ayoob Hana, Timmis Oliver G, Sang Kim-Hanh Le Quan, Genovese Federica, Imrich Richard, Rovensky Jozef, Srinivasaraghavan Rangan, Bharadwaj Shruthi K, Spiegel Ronen and Zatkova Andrea. 20160919. Twelve novel HGD gene variants identified in 99 alkaptonuria patients: focus on 'black bone disease' in Italy. : European journal of human genetics : EJHG.
Harvard
Nemethova M., Radvanszky J., Kadasi L., Ascher D. B., Pires D. E. V., Blundell T. L., Porfirio B., Mannoni A., Santucci A., Milucci L., Sestini S., Biolcati G., Sorge F., Aurizi C., Aquaron R., Alsbou M., Lourenço C. M., Ramadevi K., Ranganath L. R., Gallagher J. A., van Kan C., Hall A. K., Olsson B., Sireau N., Ayoob H., Timmis O. G., Sang K. L. Q., Genovese F., Imrich R., Rovensky J., Srinivasaraghavan R., Bharadwaj S. K., Spiegel R. and Zatkova A. (20160919). Twelve novel HGD gene variants identified in 99 alkaptonuria patients: focus on 'black bone disease' in Italy. : European journal of human genetics : EJHG.
MLA
Nemethova Martina, Radvanszky Jan, Kadasi Ludevit, Ascher David B, Pires Douglas E V, Blundell Tom L, Porfirio Berardino, Mannoni Alessandro, Santucci Annalisa, Milucci Lia, Sestini Silvia, Biolcati Gianfranco, Sorge Fiammetta, Aurizi Caterina, Aquaron Robert, Alsbou Mohammed, Lourenço Charles Marques, Ramadevi Kanakasabapathi, Ranganath Lakshminarayan R, Gallagher James A, van Kan Christa, Hall Anthony K, Olsson Birgitta, Sireau Nicolas, Ayoob Hana, Timmis Oliver G, Sang Kim-Hanh Le Quan, Genovese Federica, Imrich Richard, Rovensky Jozef, Srinivasaraghavan Rangan, Bharadwaj Shruthi K, Spiegel Ronen and Zatkova Andrea. Twelve novel HGD gene variants identified in 99 alkaptonuria patients: focus on 'black bone disease' in Italy. : European journal of human genetics : EJHG. 20160919.