(Q30649980)
Statements
1 reference
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). (English)
1 reference
F Vitelli
1 reference
M Piccini
1 reference
F Caroli
1 reference
B Franco
1 reference
A Malandrini
1 reference
B Pober
1 reference
J Jonsson
1 reference
V Sorrentino
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A Renieri
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1 February 1999
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Identifiers
1 reference