Meyer, Ricketts, Morgan et al.: "Mutations in FLVCR2 are associated with proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome (Fowler syndrome)." in: American journal of human genetics, Vol. 86, Issue 3, pp. 471-8, 2010 (PubMed).
Brown, Fung, Tailor: "Comprehensive mapping of receptor-functioning domains in feline leukemia virus subgroup C receptor FLVCR1." in: Journal of virology, Vol. 80, Issue 4, pp. 1742-51, 2006 (PubMed).
Brasier, Tikellis, Xuereb et al.: "Novel hexad repeats conserved in a putative transporter with restricted expression in cell types associated with growth, calcium exchange and homeostasis." in: Experimental cell research, Vol. 293, Issue 1, pp. 31-42, 2004 (PubMed).
Heilig, Eckenberg, Petit et al.: "The DNA sequence and analysis of human chromosome 14." in: Nature, Vol. 421, Issue 6923, pp. 601-7, 2003 (PubMed).