Eriksson M, Brown WT, Gordon LB, Glynn MW, Singer J, Scott L, Erdos MR, Robbins CM, Moses TY, Berglund P, Dutra A, Pak E, Durkin S, Csoka AB, Boehnke M, Glover TW, Collins FS (2003). «Recurrent de novo point mutations in lamin A cause Hutchinson-Gilford progeria syndrome». Nature423 (6937): 293-8. PMID12714972. doi:10.1038/nature01629.
Liu B, Wang J, Chan KM, Tjia WM, Deng W, Guan X, Huang JD, Li KM, Chau PY, Chen DJ, Pei D, Pendas AM, Cadiñanos J, López-Otín C, Tse HF, Hutchison C, Chen J, Cao Y, Cheah KS, Tryggvason K, Zhou Z (2005). «Genomic instability in laminopathy-based premature aging». Nat. Med.11 (7): 780-5. PMID15980864. doi:10.1038/nm1266.
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Eriksson M, Brown WT, Gordon LB, Glynn MW, Singer J, Scott L, Erdos MR, Robbins CM, Moses TY, Berglund P, Dutra A, Pak E, Durkin S, Csoka AB, Boehnke M, Glover TW, Collins FS (2003). «Recurrent de novo point mutations in lamin A cause Hutchinson-Gilford progeria syndrome». Nature423 (6937): 293-8. PMID12714972. doi:10.1038/nature01629.