Genotype-phenotype correlations in PCD patients carrying DNAH5 mutations.

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DOI:10.1136/thorax.58.6.552-b
作者：A Kispert, M Petry, H Olbrich, A Volz, U-P Ketelsen, J Horvath, R Melkaoui, H Omran, M Zariwala, P G Noone, M Knowles
文献类型：期刊论文
补充材料：只需要正文
文献链接：https://doi.org/10.1136/thorax.58.6.552-b

BMJ

Abstract：Primary ciliary dyskinesia (PCD) is usually inherited as an autosomal recessive disorder. Affected individuals suffer from recurrent infections of the upper and lower respiratory tract due t

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