^Jurado LA, Coloma A, Cruces J (jun 1999). „Identification of a human homolog of the Drosophila rotated abdomen gene (POMT1) encoding a putative protein O-mannosyl-transferase, and assignment to human chromosome 9q34.1”. Genomics. 58 (2): 171—80. PMID10366449. doi:10.1006/geno.1999.5819.CS1 održavanje: Format datuma (veza)
Grewal PK, Hewitt JE (oktobar 2003). „Glycosylation defects: a new mechanism for muscular dystrophy?”. Human Molecular Genetics. 12 Spec No 2 (90002): R259—64. PMID12925572. doi:10.1093/hmg/ddg272.CS1 održavanje: Format datuma (veza)
Sabatelli P, Columbaro M, Mura I, Capanni C, Lattanzi G, Maraldi NM, et al. (maj 2003). „Extracellular matrix and nuclear abnormalities in skeletal muscle of a patient with Walker-Warburg syndrome caused by POMT1 mutation”. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1638 (1): 57—62. PMID12757935. doi:10.1016/s0925-4439(03)00040-1.CS1 održavanje: Format datuma (veza)
Kim DS, Hayashi YK, Matsumoto H, Ogawa M, Noguchi S, Murakami N, et al. (mart 2004). „POMT1 mutation results in defective glycosylation and loss of laminin-binding activity in alpha-DG”. Neurology. 62 (6): 1009—11. PMID15037715. S2CID28864658. doi:10.1212/01.wnl.0000115386.28769.65.CS1 održavanje: Format datuma (veza)
Akasaka-Manya K, Manya H, Endo T (decembar 2004). „Mutations of the POMT1 gene found in patients with Walker-Warburg syndrome lead to a defect of protein O-mannosylation”. Biochemical and Biophysical Research Communications. 325 (1): 75—9. PMID15522202. doi:10.1016/j.bbrc.2004.10.001.CS1 održavanje: Format datuma (veza)
Currier SC, Lee CK, Chang BS, Bodell AL, Pai GS, Job L, et al. (februar 2005). „Mutations in POMT1 are found in a minority of patients with Walker-Warburg syndrome”. American Journal of Medical Genetics. Part A. 133A (1): 53—7. PMID15637732. S2CID16549086. doi:10.1002/ajmg.a.30487.CS1 održavanje: Format datuma (veza)
Balci B, Uyanik G, Dincer P, Gross C, Willer T, Talim B, et al. (april 2005). „An autosomal recessive limb girdle muscular dystrophy (LGMD2) with mild mental retardation is allelic to Walker-Warburg syndrome (WWS) caused by a mutation in the POMT1 gene”. Neuromuscular Disorders. 15 (4): 271—5. PMID15792865. S2CID23007648. doi:10.1016/j.nmd.2005.01.013.CS1 održavanje: Format datuma (veza)
Otsuki T, Ota T, Nishikawa T, Hayashi K, Suzuki Y, Yamamoto J, et al. (2007). „Signal sequence and keyword trap in silico for selection of full-length human cDNAs encoding secretion or membrane proteins from oligo-capped cDNA libraries”. DNA Research. 12 (2): 117—26. PMID16303743. doi:10.1093/dnares/12.2.117.
Akasaka-Manya K, Manya H, Nakajima A, Kawakita M, Endo T (jul 2006). „Physical and functional association of human protein O-mannosyltransferases 1 and 2”. The Journal of Biological Chemistry. 281 (28): 19339—45. PMID16698797. doi:10.1074/jbc.M601091200.CS1 održavanje: Format datuma (veza)
Bouchet C, Vuillaumier-Barrot S, Gonzales M, Boukari S, Bizec CL, Fallet C, et al. (januar 2007). „Detection of an Alu insertion in the POMT1 gene from three French Walker Warburg syndrome families”. Molecular Genetics and Metabolism. 90 (1): 93—6. PMID17079174. doi:10.1016/j.ymgme.2006.09.005.CS1 održavanje: Format datuma (veza)