1. Vainzof, Mariz, Souza, Lucas S, Gurgel-Giannetti, Juliana, Zatz, Mayana. 2021. Sarcoglycanopathies: an update. In Neuromuscular disorders : NMD, 31, 1021-1027. doi:10.1016/j.nmd.2021.07.014. https://pubmed.ncbi.nlm.nih.gov/34404573/
2. Ten Dam, Leroy, Frankhuizen, Wendy S, Linssen, Wim H J P, van der Kooi, Anneke J, Ginjaar, Ieke. 2019. Autosomal recessive limb-girdle and Miyoshi muscular dystrophies in the Netherlands: The clinical and molecular spectrum of 244 patients. In Clinical genetics, 96, 126-133. doi:10.1111/cge.13544. https://pubmed.ncbi.nlm.nih.gov/30919934/
3. Perez-Ortiz, Andric Christopher, Luna-Angulo, Alexandra, Zenteno, Juan Carlos, Jacob-Kuttothara, Stefany, Estrada-Mena, Francisco Javier. 2018. Significant Association Between Variant in SGCD and Age-Related Macular Degeneration. In Genes, 9, . doi:10.3390/genes9100467. https://pubmed.ncbi.nlm.nih.gov/30257524/
4. Perez-Ortiz, Andric C, Peralta-Ildefonso, Martha J, Lira-Romero, Esmeralda, Coral-Vázquez, Ramón M, Estrada-Mena, Francisco J. 2019. Lack of Delta-Sarcoglycan (Sgcd) Results in Retinal Degeneration. In International journal of molecular sciences, 20, . doi:10.3390/ijms20215480. https://pubmed.ncbi.nlm.nih.gov/31689918/
5. Bauer, Ralf, Enns, Helene, Jungmann, Andreas, Katus, Hugo A, Müller, Oliver J. 2018. Various effects of AAV9-mediated βARKct gene therapy on the heart in dystrophin-deficient (mdx) mice and δ-sarcoglycan-deficient (Sgcd-/-) mice. In Neuromuscular disorders : NMD, 29, 231-241. doi:10.1016/j.nmd.2018.12.006. https://pubmed.ncbi.nlm.nih.gov/30782477/
6. Brunetti, Barbara, Bacci, Barbara, Abbate, Jessica Maria, Leeb, Tosso, Drögemüller, Michaela. 2023. SGCD Missense Variant in a Lagotto Romagnolo Dog with Autosomal Recessively Inherited Limb-Girdle Muscular Dystrophy. In Genes, 14, . doi:10.3390/genes14081641. https://pubmed.ncbi.nlm.nih.gov/37628692/