Clinical and genetic analysis of two patients with primary ciliary dyskinesia caused by a novel variant of DNAAF2
Abstract Background The study describes the clinical manifestations and variant screening of two Chinese siblings with primary ciliary dyskinesia (PCD). They carry the same DNAAF2 genotype, which is an extremely rare PCD genotype in the Chinese population. In addition, the study illustrated an overv...
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| Main Authors: | , , , , , , , , |
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| Format: | Book |
| Published: |
BMC,
2023-12-01T00:00:00Z.
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| Subjects: | |
| Online Access: | Connect to this object online. |
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