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俭朴的语琴
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2024-10-02 加入
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A novel de novo TMEM63A variant in a patient with severe hypomyelination and global developmental delay
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Spinal cord involvement and paroxysmal events in “Infantile Onset Transient Hypomyelination” due to TMEM63A mutation
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Identification of a novel cell cycle regulated gene, HURP, overexpressed in human hepatocellular carcinoma
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The hidden weavers: A review of DNA/RNA R-loops in stem cell biology and therapeutic potential
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2个月前
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The first familial case of inherited intellectual developmental disorder with dysmorphic facies and behavioral abnormalities (IDDFBA) with a novel FBXO11 variant
3个月前
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High diagnostic yield of syndromic intellectual disability by targeted next-generation sequencing
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Mental health problems in children with intellectual disability
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Human embryonic stem cells
3个月前
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FBXO11 amplifies type I interferon signaling to exert antiviral effects by facilitating the assemble of TRAF3-TBK1-IRF3 complex
3个月前
已完结
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标题错误
3个月前
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