A human integrin-α3 mutation confers major renal developmental defects.. Homo sapiens
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https://www.ncbi.nlm.nih.gov/bioproject/PRJNA236572
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资源简介：
Integrin-α3 plays a central role in the interplay of cells, morphogens and ECM, required for proper nephrogenesis, thus adding ITGA3 to the list of CAKUT (congenital anomalies of the kidney and urinary tract)-causing genes. Overall design: we used renal tissue originally obtained from a patient with an ITGA3 mutation and assessed its gene expression profile as compared to controls
创建时间：
2014-01-20
