APA

Banka S., de Goede C., Yue W. W., Morris A. A. M., von Bremen B., Chandler K. E., Feichtinger R. G., Hart C., Khan N., Lunzer V., Mataković L., Marquardt T., Makowski C., Prokisch H., Debus O., Nosaka K., Sonwalkar H., Zimmermann F. A., Sperl W. & Mayr J. A. (20150716). Expanding the clinical and molecular spectrum of thiamine pyrophosphokinase deficiency: a treatable neurological disorder caused by TPK1 mutations. : Molecular genetics and metabolism.

Chicago

Banka Siddharth, de Goede Christian, Yue Wyatt W, Morris Andrew A M, von Bremen Beate, Chandler Kate E, Feichtinger René G, Hart Claire, Khan Nasaim, Lunzer Verena, Mataković Lavinija, Marquardt Thorsten, Makowski Christine, Prokisch Holger, Debus Otfried, Nosaka Kazuto, Sonwalkar Hemant, Zimmermann Franz A, Sperl Wolfgang and Mayr Johannes A. 20150716. Expanding the clinical and molecular spectrum of thiamine pyrophosphokinase deficiency: a treatable neurological disorder caused by TPK1 mutations. : Molecular genetics and metabolism.

Harvard

Banka S., de Goede C., Yue W. W., Morris A. A. M., von Bremen B., Chandler K. E., Feichtinger R. G., Hart C., Khan N., Lunzer V., Mataković L., Marquardt T., Makowski C., Prokisch H., Debus O., Nosaka K., Sonwalkar H., Zimmermann F. A., Sperl W. and Mayr J. A. (20150716). Expanding the clinical and molecular spectrum of thiamine pyrophosphokinase deficiency: a treatable neurological disorder caused by TPK1 mutations. : Molecular genetics and metabolism.

MLA

Banka Siddharth, de Goede Christian, Yue Wyatt W, Morris Andrew A M, von Bremen Beate, Chandler Kate E, Feichtinger René G, Hart Claire, Khan Nasaim, Lunzer Verena, Mataković Lavinija, Marquardt Thorsten, Makowski Christine, Prokisch Holger, Debus Otfried, Nosaka Kazuto, Sonwalkar Hemant, Zimmermann Franz A, Sperl Wolfgang and Mayr Johannes A. Expanding the clinical and molecular spectrum of thiamine pyrophosphokinase deficiency: a treatable neurological disorder caused by TPK1 mutations. : Molecular genetics and metabolism. 20150716.