. Author manuscript; available in PMC: 2010 Oct 26.

Published in final edited form as: Exp Cell Res. 2007 Mar 30;313(10):2121–2133. doi: 10.1016/j.yexcr.2007.03.028

Table 3.

Diseases caused by mutations in genes encoding lamin-associated proteins of the inner nuclear. On-line Mendelian Inheritance in Man entry numbers are given in parentheses.

EMD

X-linked Emery-Dreifuss Muscular Dystrophy (#310300)

LBR

Pelger-Huet Anomaly, Autosomal Recessive (#169400)

Hydrops-Ectopic Calcification-Moth-Eaten Skeletal Dysplasia (HEM)/Greenberg Skeletal Dysplasia, Autosomal Dominant (#215140)

LEMD3 (MAN1)

Buschke-Ollendorff Syndrome, Autosomal Recessive (#166700)

Melorheostosis, Familial and Melorheostosis with Osteopoikilosis, Autosomal Recessive (#155950)