Brockington, M., Blake, D. J., Prandini, P., Brown, S. C., Torelli, S., Benson, M. A., . . . Muntoni, F. (2001). Mutations in the Fukutin-Related Protein Gene (FKRP) Cause a Form of Congenital Muscular Dystrophy with Secondary Laminin α2 Deficiency and Abnormal Glycosylation of α-Dystroglycan. The American Society of Human Genetics.
Chicago-tyylinen lähdeviittausBrockington, Martin, et al. Mutations in the Fukutin-Related Protein Gene (FKRP) Cause a Form of Congenital Muscular Dystrophy With Secondary Laminin α2 Deficiency and Abnormal Glycosylation of α-Dystroglycan. The American Society of Human Genetics, 2001.
MLA-viiteBrockington, Martin, et al. Mutations in the Fukutin-Related Protein Gene (FKRP) Cause a Form of Congenital Muscular Dystrophy With Secondary Laminin α2 Deficiency and Abnormal Glycosylation of α-Dystroglycan. The American Society of Human Genetics, 2001.