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)

✍ Scribed by Francesca Vitelli; Monica Piccini; Francesco Caroli; Brunella Franco; Alessandro Malandrini; Barbara Pober; Jon Jonsson; Vincenzo Sorrentino; Alessandra Renieri

• Book ID: 115614596
• Publisher: Elsevier Science
• Year: 1999
• Tongue: English
• Weight: 165 KB
• Volume: 55
• Category: Article
• ISSN: 0888-7543
• DOI: 10.1006/geno.1998.5666