Associated Papers
Novel compound heterozygous mutation in DNAH9 causes complex congenital heart disease.
Liu X et al.
Molecular Medicine Reports, 2025
DNAH9 variants in children with post-infectious bronchiolitis/bronchitis obliterans.
Guan Y et al.
Orphanet Journal of Rare Diseases, 2025
Whole exome sequencing analysis of 167 men with primary infertility.
Zhou H et al.
Bmc Medical Genomics, 2024
A family with normal sperm motility carrying a sY86 deletion in AZFa region and partial deletion in AZFc region.
Zhao Y et al.
Frontiers in Genetics, 2024
Biallelic DNAH9 mutations are identified in Chinese patients with defective left-right patterning and cilia-related complex congenital heart disease.
Chen W et al.
Human Genetics, 2022
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