Late Breaking Abstract - Whole exome sequencing and runs of homozygosity Identifies a Novel Mutation of DYX1C1 in Primary Ciliary Dyskinesia From a consanguineous Chinese Family

T. Guo (chang sha, China)

Source: International Congress 2017 – Late-breaking findings in pulmonary diseases
Session: Late-breaking findings in pulmonary diseases
Session type: Thematic Poster
Number: 2804
Disease area: Paediatric lung diseases

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T. Guo (chang sha, China). Late Breaking Abstract - Whole exome sequencing and runs of homozygosity Identifies a Novel Mutation of DYX1C1 in Primary Ciliary Dyskinesia From a consanguineous Chinese Family. 2804

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