蛛网膜
Camptodactyly公司
挛缩
马凡氏综合征
医学
发病机制
结缔组织
脊柱侧凸
遗传学
病理
生物
解剖
外科
标识
DOI:10.1080/03008207.2024.2340004
摘要
This study enriched the pathogenic spectrum of CCA and identified a hotspot region in FBN2 gene associated with severe cardiovascular manifestations. We recommend that patients carrying pathogenic variants in exons 31 to 35 of FBN2 pay more attention to cardiac evaluation.
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