Z. Ahmad, E. Zackai, and L. Medne, Early onset mandibuloacral dysplasia due to compound heterozygous mutations in ZMPSTE24, American Journal of Medical Genetics Part A, vol.146, issue.11, 2010.
DOI : 10.1590/S0004-27302008000800008

D. Araújo-vilar, J. Lado-abeal, and F. Palos-paz, A novel phenotypic expression associated with a new mutation in LMNA gene, characterized by partial lipodystrophy, insulin resistance, aortic stenosis and hypertrophic cardiomyopathy, Clinical Endocrinology, vol.114, issue.1, pp.61-69, 2008.
DOI : 10.1093/hmg/ddi158

G. Bonne, D. Barletta, M. Varnous, and S. , Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy, Nature Genetics, vol.21, issue.3, pp.285-293, 1999.
DOI : 10.1038/6799

D. Sandre-giovannoli, A. Bernard, R. Cau, and P. , Lamin A Truncation in Hutchinson-Gilford Progeria, Science, vol.300, issue.5628, p.2055, 2003.
DOI : 10.1126/science.1084125

Y. Doubaj, D. Sandre-giovannoli, A. Vera, and E. , An inherited LMNA gene mutation in atypical progeria syndrome, Am J Med Genet A, vol.158, pp.2881-2888, 2012.

M. Eriksson, W. Brown, and L. Gordon, Recurrent de novo point mutations in lamin A cause Hutchinson???Gilford progeria syndrome, Nature, vol.66, issue.6937, pp.293-301, 2003.
DOI : 10.1086/302836

H. Gottron, Famili??re Akrogerie, Archiv f??r Dermatologie und Syphilis, vol.81, issue.5, p.571, 1940.
DOI : 10.1007/BF01828361

C. Hashimoto, M. Abe, and N. Onozawa, Acrogeria (Gottron type): a vascular disorder?, British Journal of Dermatology, vol.42, issue.2, pp.497-501, 2004.
DOI : 10.1111/j.1346-8138.1993.tb01341.x

T. Jansen, A. De-paepe, and N. Luytinck, COL3A1 mutation leading to acrogeria (Gottron type), British Journal of Dermatology, vol.91, issue.1, pp.178-80, 2000.
DOI : 10.1046/j.1365-2133.1996.d01-971.x

M. Kane, M. Lindsay, and D. Judge, -associated cardiocutaneous progeria: An inherited autosomal dominant premature aging syndrome with late onset, American Journal of Medical Genetics Part A, vol.146, issue.7, pp.1599-611, 2013.
DOI : 10.1002/ajmg.a.32259
URL : http://onlinelibrary.wiley.com/doi/10.1002/ajmg.a.35971/pdf

G. Novelli, A. Muchir, and F. Sangiuolo, Mandibuloacral Dysplasia Is Caused by a Mutation in LMNA-Encoding Lamin A/C, The American Journal of Human Genetics, vol.71, issue.2, 2002.
DOI : 10.1086/341908

F. Pope, P. Narcisi, and A. Nicholls, COL3A1 mutations cause variable clinical phenotypes including acrogeria and vascular rupture, British Journal of Dermatology, vol.51, issue.7, pp.163-81, 1996.
DOI : 10.1016/S0140-6736(83)92631-4

M. Prokocimer, M. Davidovich, and M. Nissim-rafinia, Nuclear lamins: key regulators of nuclear structure and activities, Journal of Cellular and Molecular Medicine, vol.17, issue.6, pp.1059-85, 2009.
DOI : 10.1002/ajmg.a.31803

K. Schreiber and B. Kennedy, When Lamins Go Bad: Nuclear Structure and Disease, Cell, vol.152, issue.6, pp.1365-75, 2013.
DOI : 10.1016/j.cell.2013.02.015
URL : https://doi.org/10.1016/j.cell.2013.02.015