Heterozygous variants in MYH10 associated with neurodevelopmental disorders and congenital anomalies with evidence for primary cilia-dependent defects in Hedgehog signaling.
Heterozygous variants in MYH10 associated with neurodevelopmental disorders and congenital anomalies with evidence for primary cilia-dependent defects in Hedgehog signaling.
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DOI：
10.1016/j.gim.2022.07.005
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发表时间：
2022-08
期刊：
影响因子：
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通讯作者：
Alexander M. Holtz;Rachel Vancoil;Elizabeth A VanSickle;D. A. Carere;Kara A. Withrow;E. Torti;J. Juusola-J.
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文献类型：
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作者：
Alexander M. Holtz;Rachel Vancoil;Elizabeth A VanSickle;D. A. Carere;Kara A. Withrow;E. Torti;J. Juusola-J.
