A homozygous FKRP start codon mutation is associated with Walker–Warburg syndrome, the severe end of the clinical spectrum.

MLA

van Reeuwijk, J., et al. “A Homozygous FKRP Start Codon Mutation Is Associated with Walker–Warburg Syndrome, the Severe End of the Clinical Spectrum.” Clinical Genetics, vol. 78, no. 3, Sept. 2010, pp. 275–81. EBSCOhost, https://doi.org/10.1111/j.1399-0004.2010.01384.x.

APA

van Reeuwijk, J., Olderode-Berends, M. J. W., van den Elzen, C., Brouwer, O. F., Roscioli, T., van Pampus, M. G., Scheffer, H., Brunner, H. G., van Bokhoven, H., & Hol, F. A. (2010). A homozygous FKRP start codon mutation is associated with Walker–Warburg syndrome, the severe end of the clinical spectrum. Clinical Genetics, 78(3), 275–281. https://doi.org/10.1111/j.1399-0004.2010.01384.x

Chicago

van Reeuwijk, J., M. J. W. Olderode-Berends, C. van den Elzen, O. F. Brouwer, T. Roscioli, M. G. van Pampus, H. Scheffer, H. G. Brunner, H. van Bokhoven, and F. A. Hol. 2010. “A Homozygous FKRP Start Codon Mutation Is Associated with Walker–Warburg Syndrome, the Severe End of the Clinical Spectrum.” Clinical Genetics 78 (3): 275–81. doi:10.1111/j.1399-0004.2010.01384.x.