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Hutchinson-Gilford syndrome |
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This PA is a new initiative to support research to understand how mutations in the gene for lamin A/C affect nuclear structure, thus leading to bothdysfunction of the nuclear envelope, and depending on the mutation, Hutchinson-Gilford syndrome in humans (Eriksson et al. These range from Down Syndrome (1 in 660 live births) to Hutchinson-Gilford Syndrome (1 in 250,000 live births). |
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