Fresquet, Jowitt, Ylöstalo, Coffey, Meadows, Ala-Kokko, Thornton, Briggs: "Structural and functional characterization of recombinant matrilin-3 A-domain and implications for human genetic bone diseases." in: The Journal of biological chemistry, Vol. 282, Issue 48, pp. 34634-43, 2007 (PubMed).
Liu, Jin, Cao, Zhao, Lin, Sun: "[Analysis of association between COL9A1 gene and idiopathic congenital talipes equinovarus]." in: Yi chuan = Hereditas / Zhongguo yi chuan xue hui bian ji, Vol. 29, Issue 4, pp. 427-32, 2007 (PubMed).
Van Camp, Snoeckx, Hilgert, van den Ende, Fukuoka, Wagatsuma, Suzuki, Smets, Vanhoenacker, Declau, Van de Heyning, Usami: "A new autosomal recessive form of Stickler syndrome is caused by a mutation in the COL9A1 gene." in: American journal of human genetics, Vol. 79, Issue 3, pp. 449-57, 2006 (PubMed).
Sivakumaran, Resendes, Robertson, Giersch, Morton: "Characterization of an abundant COL9A1 transcript in the cochlea with a novel 3' UTR: Expression studies and detection of miRNA target sequence." in: Journal of the Association for Research in Otolaryngology : JARO, Vol. 7, Issue 2, pp. 160-72, 2006 (PubMed).