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WHOLE‐EXOME SEQUENCING AND RUNS OF HOMOZYGOSITY IDENTIFIES A NOVEL MUTATION OF DYX1C1 IN PRIMARY CILIARY DYSKINESIA FROM AN INBRED CHINESE FAMILY
Publication year - 2017
Publication title -
respirology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.857
H-Index - 85
eISSN - 1440-1843
pISSN - 1323-7799
DOI - 10.1111/resp.13207_225
Subject(s) - primary ciliary dyskinesia , exome sequencing , mutation , genetics , medicine , genealogy , biology , gene , history , bronchiectasis , lung
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