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Vitelli, F., Piccini, M., Caroli, F., Franco, B., Malandrini, A., Pober, B., et al. (1999) Identification and Characterization of a Highly Conserved Protein Absent in the Alport Syndrome (A), Mental Retardation (M), Midface Hypoplasia (M), and Elliptocytosis (E) Contiguous Gene Deletion Syndrome (AMME). Genomics, 55, 335-340. https://doi.org/10.1006/geno.1998.5666

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