Mouse model for microcephaly associated with a defect in erythropoiesis
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https://www.ncbi.nlm.nih.gov/bioproject/PRJNA949436
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资源简介：
The frequency of syndromic associations between brain developmental abnormalities and haematological developmental abnormalities suggests the existence of common and limiting pathways in neurogenesis and haematopoiesis. In order to identify common pathophysiological mechanisms, we focused our research on a model of primary microcephaly in the Mcph1 knockout mouse.
创建时间：
2023-03-28
