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)

Author： Vitelli F.   Piccini M.   Caroli F.   Franco B.   Malandrini A.   Pober B.   Jonsson J.   Sorrentino V.   Renieri A.  

Publisher： Elsevier

ISSN： 0888-7543

Source： Genomics, Vol.55, Iss.3, 1999-02, pp. : 335-340

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