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Homozygosity for a missense mutation in fibulin-5 (FBLN5) results in a severe form of cutis laxa.

(2002) HUMAN MOLECULAR GENETICS. 11(18). p.2113-2118
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Chicago
Loeys, Bart, L VAN MALDERGEM, Geert Mortier, Paul Coucke, S GERNIERS, Jean Naeyaert, and Anne De Paepe. 2002. “Homozygosity for a Missense Mutation in Fibulin-5 (FBLN5) Results in a Severe Form of Cutis Laxa.” Human Molecular Genetics 11 (18): 2113–2118.
APA
Loeys, Bart, VAN MALDERGEM, L., Mortier, G., Coucke, P., GERNIERS, S., Naeyaert, J., & De Paepe, A. (2002). Homozygosity for a missense mutation in fibulin-5 (FBLN5) results in a severe form of cutis laxa. HUMAN MOLECULAR GENETICS, 11(18), 2113–2118.
Vancouver
1.
Loeys B, VAN MALDERGEM L, Mortier G, Coucke P, GERNIERS S, Naeyaert J, et al. Homozygosity for a missense mutation in fibulin-5 (FBLN5) results in a severe form of cutis laxa. HUMAN MOLECULAR GENETICS. 2002;11(18):2113–8.
MLA
Loeys, Bart, L VAN MALDERGEM, Geert Mortier, et al. “Homozygosity for a Missense Mutation in Fibulin-5 (FBLN5) Results in a Severe Form of Cutis Laxa.” HUMAN MOLECULAR GENETICS 11.18 (2002): 2113–2118. Print.
@article{156478,
  author       = {Loeys, Bart and VAN MALDERGEM, L and Mortier, Geert and Coucke, Paul and GERNIERS, S and Naeyaert, Jean and De Paepe, Anne},
  issn         = {0964-6906},
  journal      = {HUMAN MOLECULAR GENETICS},
  language     = {eng},
  number       = {18},
  pages        = {2113--2118},
  title        = {Homozygosity for a missense mutation in fibulin-5 (FBLN5) results in a severe form of cutis laxa.},
  volume       = {11},
  year         = {2002},
}

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