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Recurrent De Novo Point Mutations in Lamin A Cause Hutchinson-Gilford Progeria Syndrome

Gao SS, Li DY, Huo ZK, Zhang YL, Cao YZ, Tan YY, et al

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(2) low-volume MS-LTC-DRGs (that is, MS-LTC-DRGs that contain between 1 and 24 applicable LTCH cases that are grouped into quintiles (as described later in this section in Step 3 of our proposed methodology) and assigned the relative weight of the quintile)

(57) analyzed ferroptosis-related gene expression patterns specifically in myocardium following coronary occlusion, revealing an immune-ferroptosis axis that influences post-infarction remodeling

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