A novel missense mutation in the SH2 domain of the STAT5B gene results in a transcriptionally inactive STAT5b associated with severe IGF-I deficiency, immune dysfunction, and lack of pulmonary disease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

A novel missense mutation in the SH2 domain of the STAT5B gene results in a transcriptionally inactive STAT5b associated with severe IGF-I deficiency, immune dysfunction, and lack of pulmonary disease

Authors:	Scaglia Paula A Martínez Alicia S Feigerlová Eva Bezrodnik Liliana Gaillard María Isabel Di Giovanni Daniela Ballerini María Gabriela Jasper Héctor G Heinrich Juan J Fang Peng Domené Horacio M Rosenfeld Ron G Hwa Vivian

Affiliation:	Centro de Investigaciones Endocrinológicas (Consejo Nacional de Investigaciones Científicas y Técnicas), Ricardo Gutiérrez Children's Hospital, 1330 Buenos Aires, Argentina.

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