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120 积分 2026-01-21 加入
Heterozygous loss-of-function variant in METTL5 is associated with intellectual disability
12小时前
已关闭
Ribosome heterogeneity in stem cells and development
1个月前
已关闭
Genetics of human brain development
1个月前
已完结
METTL5 deficiency induces oligoasthenoteratozoospermia via impaired 18S rRNA m6A methylation in humans and mice
3个月前
已完结
Integration of multi-omics summary data reveals the role of N6-methyladenosine in neuropsychiatric disorders
3个月前
已完结
Microcephaly-related global developmental delay caused by a pathogenic METTL5 splicing mutation in a Chinese family
3个月前
已完结
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