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1100 积分 2023-11-27 加入
Neuropathy and myopathy: an under-recognized phenotypic convergence in rare genetic disorders
1小时前
已完结
A first for CRISPR: powerful prime editing alters DNA directly in the human body
7天前
已关闭
Multimodal KCNQ1 Variant-Effect Maps Define Ion Channel Mechanisms and Disease Risk
8天前
已完结
Leveraging genomic deep learning models for the prediction of noncoding variant effects
8天前
已完结
The genetic architecture of pentanucleotide repeat variation and disease association
13天前
已完结
Inheritance and selection of the mitochondrial genome
24天前
已完结
No bird soars in a calm: therapeutic germline gene editing
29天前
已完结
Protein trans-splicing: Solving the challenge of gene therapy for large genes
1个月前
已完结
From N-of-1 therapy to health-system implementation
1个月前
已完结
The difficulties of developing guidelines for rare disease: where consensus, evidence-based medicine and screening principles conflict
1个月前
已关闭
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