APA

Iqbal Z., Shahzad M., Vissers L. E. L. M., van Scherpenzeel M., Gilissen C., Razzaq A., Zahoor M. Y., Khan S. N., Kleefstra T., Veltman J. A., de Brouwer A. P. M., Lefeber D. J., van Bokhoven H. & Riazuddin S. (20131029). A compound heterozygous mutation in DPAGT1 results in a congenital disorder of glycosylation with a relatively mild phenotype. : European journal of human genetics : EJHG.

Chicago

Iqbal Zafar, Shahzad Mohsin, Vissers Lisenka E L M, van Scherpenzeel Monique, Gilissen Christian, Razzaq Attia, Zahoor Muhammad Yasir, Khan Shaheen N, Kleefstra Tjitske, Veltman Joris A, de Brouwer Arjan P M, Lefeber Dirk J, van Bokhoven Hans and Riazuddin Sheikh. 20131029. A compound heterozygous mutation in DPAGT1 results in a congenital disorder of glycosylation with a relatively mild phenotype. : European journal of human genetics : EJHG.

Harvard

Iqbal Z., Shahzad M., Vissers L. E. L. M., van Scherpenzeel M., Gilissen C., Razzaq A., Zahoor M. Y., Khan S. N., Kleefstra T., Veltman J. A., de Brouwer A. P. M., Lefeber D. J., van Bokhoven H. and Riazuddin S. (20131029). A compound heterozygous mutation in DPAGT1 results in a congenital disorder of glycosylation with a relatively mild phenotype. : European journal of human genetics : EJHG.

MLA

Iqbal Zafar, Shahzad Mohsin, Vissers Lisenka E L M, van Scherpenzeel Monique, Gilissen Christian, Razzaq Attia, Zahoor Muhammad Yasir, Khan Shaheen N, Kleefstra Tjitske, Veltman Joris A, de Brouwer Arjan P M, Lefeber Dirk J, van Bokhoven Hans and Riazuddin Sheikh. A compound heterozygous mutation in DPAGT1 results in a congenital disorder of glycosylation with a relatively mild phenotype. : European journal of human genetics : EJHG. 20131029.