Associated Papers
Case Report: Identification of a Novel ODAD3 Variant in a Patient With Primary Ciliary Dyskinesia.
Wang R et al.
Frontiers in Genetics, 2021
33719352 (PubMed )
Supplement: Table_2.xlsx › Table_S2
Identification of a frame shift mutation in the CCDC151 gene in a Han-Chinese family with Kartagener syndrome.
Deng S et al.
Bioscience Reports, 2020
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