SLC25A1 regulates placental development to ensure embryonic heart morphogenesis.

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DOI:10.1242/dev.204290
作者：Wenli Fan,?Zixuan Li,?Xueke He,?Xiaodong Wang,?Ming Sun,?Zhongzhou Yang
文献类型：期刊论文
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Abstract：22q11.2 deletion syndrome (22q11.2DS) is the most common chromosomal microdeletion syndrome. Congenital heart defects are prevalent in 22q11.2DS but the etiology is still poorly understood.

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