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Compound heterozygosity for mutations in LMNA causes a progeria syndrome without prelamin A accumulation
V.L.R.M. Verstraeten, J.L.V. Broers, M.A.M Steensel, van, S. Zinn-Justin, F.C.S. Ramaekers, P.M. Steijlen, M.A. Kamps, H.J.H. Kuijpers, D. Merckx, H.J.M. Smeets, R.C.M. Hennekam, C.L.M. Marcelis, A. Wijngaard, van den
Research output: Contribution to journal › Article › Academic › peer-review
85
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(Scopus)