Associated Papers
The role of SLC26A8 homozygous variants in male infertility and flagellum abnormalities.
Mao B et al.
Asian Journal of Andrology, 2024
A case report of neonatal incontinentia pigmenti complicated by severe cerebrovascular lesions in one of the male monozygotic twins.
Lin X et al.
Frontiers in Pediatrics, 2024
38832002 (PubMed )
Supplement: Table1.xlsx › filter_variants
Whole genome sequencing identifies genetic variants associated with neurogenic inflammation in rosacea.
Deng Z et al.
Nature Communications, 2023
37402769 (PubMed )
Supplement: 41467_2023_39761_MOESM4_ESM.xlsx › Sheet1
Exome sequencing in fetuses with short long bones detected by ultrasonography: A retrospective cohort study.
Huang Y et al.
Frontiers in Genetics, 2023
36923788 (PubMed )
Supplement: Table3.xlsx › Sheet1
The heterozygous mutations of SLC26A8 are not the main actors for male infertility.
Liu M et al.
Human Mutation, 2022
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