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Publication : 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).

First Author  Vitelli F Year  1999
Journal  Genomics Volume  55
Issue  3 Pages  335-40
PubMed ID  10049589 Mgi Id 
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