Associated Papers
Novel compound heterozygous mutation in DNAH9 causes complex congenital heart disease.
Liu X et al.
Molecular Medicine Reports, 2025
40376972 (PubMed )
Supplement: Supplementary_Data2.pdf
A Novel DNAH9 Gene Mutation Causing Primary Ciliary Dyskinesia With an Unusual Association of Jejunal Atresia in a Bahraini Child.
Isa HM et al.
Cureus, 2022
Clustering of Genetic Anomalies of Cilia Outer Dynein Arm and Central Apparatus in Patients with Transposition of the Great Arteries.
De Ita M et al.
Genes, 2022
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
Use of HLA peptidomics and whole exome sequencing to identify human immunogenic neo-antigens.
Kalaora S et al.
Oncotarget, 2016
26819371 (PubMed )
Supplement: oncotarget-07-5110-s002.xlsx › Genome_sequencing
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