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)期刊界 All Journals 搜尽天下杂志传播学术成果专业期刊搜索期刊信息化学术搜索

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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)

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

Institution:	Genetica Medica, Policlinico Le Scotte, Siena, Italy.

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