Associated Papers
Novel biallelic DNHD1 variants associated with male infertility with severe MMAF phenotype.
Uddin I et al.
Asian Journal of Andrology, 2025
Different Contribution of Missense and Loss-of-Function Variants to the Genetic Structure of Familial and Sporadic Meniere Disease.
Parra-Perez AM et al.
Medcomm, 2025
40989574 (PubMed )
Supplement: MCO2-6-e70394-s001.xlsx › TableS13
Exome sequencing shows same pattern of clonal tumor mutational burden, intratumor heterogenicity and clonal neoantigen between autologous tumor and Vigil product.
Willoughby D et al.
Scientific Reports, 2025
40082566 (PubMed )
Supplement: 41598_2025_90136_MOESM2_ESM.xlsx › Clonal-variants-table
The Molecular Basis of Multiple Morphological Abnormalities of Sperm Flagella and Its Impact on Clinical Practice.
Zhou Y et al.
Genes, 2024
New Mutations in DNHD1 Cause Multiple Morphological Abnormalities of the Sperm Flagella.
Martinez G et al.
International Journal of Molecular Sciences, 2023
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