Technical Articles

LDS1B
LDS1B：临床特征、分子机制与诊疗进展
LDS1B: Clinical features, molecular mechanisms, and diagnostic and therapeutic progress
发布时间 2025-07-21
LDS1B (Loeys Dietz Syndrome Type 1B) is an important subtype of Loeys Dietz Syndrome (LDS) caused by TGFBR2 gene mutations, accounting for 20% -30% of all LDS cases
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  • Immunity/Inflamma
  • LDS1B
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