Clinical and molecular genetic diagnosis of primary ciliary dyskinesia. Human associated mutation in the DNAH11 gene
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下载链接：
https://www.ncbi.nlm.nih.gov/bioproject/PRJNA801086
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资源简介：
Primary ciliary dyskinesia (PCD) is a rare genetically heterogeneous disorder of motile cilia. To date, although several PCD-associated genes have been identified, the genetic bases of most cases of PCD remain elusive.
创建时间：
2022-01-27
