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Whole-genome Sequencing Reveals a Novel Structural Variant of CCDC39 in a Term Neonate with Primary Ciliary Dyskinesia.
Annals of Laboratory Medicine ( IF 4.0 ) Pub Date : 2022-07-01 , DOI: 10.3343/alm.2022.42.4.500
Jun Hee Shin 1 , Sae-Mi Lee 2, 3 , Hyun Ho Kim 1, 4, 5 , Jin Kyu Kim 1, 4, 5
Affiliation  



中文翻译:

全基因组测序揭示了患有原发性纤毛运动障碍的新生儿中 CCDC39 的一种新的结构变体。

更新日期:2022-02-19
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