1. Abbassi, V., Lowe, C. U., & Calcagno, P. L. (1968). Oculo-cerebro-renal syndrome: A review. American Journal of Diseases of Children, 115, 143–168.
2. Al-Uzri, A. (2014). Oculocerebrorenal dystrophy (Lowe syndrome). Medscape Reference. Updated 2 Dec 2014. Available at:
http://emedicine.medscape.com/article/946043-overview
3. Allmendinger, A. M., Desai, N. S., Burke, A T., et al. (2014). Neuroimaging and renal ultrasound manifestations of oculocerebrorenal syndrome of Lowe. Radiology Case, 8, 1–7.
4. Attree, O., Olivos, I. M., Okabe, I., et al. (1992). The Lowe’s oculocerebrorenal syndrome gene encodes a protein highly homologous to inositol polyphosphate-5-phosphatase. Nature, 358, 239–242.
5. Bickel, H., & Thursby-Pelnam, D. C. (1954). Hyper-amino-aciduria in Lignac Fanconi disease, in galactosemia and in an Obscure syndrome. Archives of Disease in Childhood, 29, 224–231.