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C. Godfrey et al.: Refining genotype phenotype correlations in muscular dystrophies with defective glycosylation of dystroglycan. In: Brain. 130 (Pt 10), Oktober 2007, S.2725–2735, doi:10.1093/brain/awm212, PMID 17878207.
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O. Ibraghimov-Beskrovnaya, A. Milatovich, T. Ozcelik, B. Yang, K. Koepnick, U. Francke und K. P. Campbell: Human dystroglycan: skeletal muscle cDNA, genomic structure, origin of tissue specific isoforms and chromosomal localization. In: Human Molecular Genetics. 2. Jahrgang, Nr.10, Oktober 1993, S.1651–1657, PMID 8268918.
O. Ibraghimov-Beskrovnaya, J. M. Ervasti, C. J. Leveille, C. A. Slaughter, S. W. Sernett und K. P. Campbell: Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrix. In: Nature. 355. Jahrgang, S.6362, doi:10.1038/355696a0, PMID 1741056.
C. Godfrey et al.: Refining genotype phenotype correlations in muscular dystrophies with defective glycosylation of dystroglycan. In: Brain. 130 (Pt 10), Oktober 2007, S.2725–2735, doi:10.1093/brain/awm212, PMID 17878207.
K. Matsumura, I. Nonaka und K. P. Campbell: Abnormal expression of dystrophin-associated proteins in Fukuyama-type congenital muscular dystrophy. In: The Lancent. 341. Jahrgang, Nr.8844, Februar 1993, S.521–522, doi:10.1016/0140-6736(93)90279-P, PMID 8094772.
