【罕見疾病】結合基因組、表現型、功能、結構和DL，分析MCT8變異與疾病嚴重程度的關係

 【罕見疾病】結合基因組、表現型、功能、結構和DL，分析MCT8變異與疾病嚴重程度的關係

 文章出處  

Nature Communications 

 

 原文標題  

Mapping variants in thyroid hormone transporter MCT8 to disease severity by genomic, phenotypic, functional, structural and deep learning integration 

 

 文章序號  

7527 

 

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