Associated Papers
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
Exploring the Structural and Functional Effects of Nonsynonymous SNPs in the Human Serotonin Transporter Gene Through In Silico Approaches.
Mia MA et al.
Bioinformatics and Biology Insights, 2022
Identification of six polymorphisms as novel susceptibility loci for ischemic or hemorrhagic stroke by exome-wide association studies.
Yamada Y et al.
International Journal of Molecular Medicine, 2017
Association between polymorphisms in the human serotonin transporter gene and lifelong premature ejaculation in the Han population.
Peng DW et al.
Asian Journal of Andrology, 0
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