Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   

Homozygous missense mutation in the lamin A/C gene causes autosomal recessive Hutchinson-Gilford progeria syndrome.

Authors: Plasilova, M  Chattopadhyay, C  Pal, P  Schaub, NA  Buechner, SA  Mueller, H  Miny, P  Ghosh, A  Heinimann, K 
Citation: Plasilova M, etal., J Med Genet. 2004 Aug;41(8):609-14.
Pubmed: (View Article at PubMed) PMID:15286156
DOI: Full-text: DOI:10.1136/jmg.2004.019661



Disease Annotations
Phenotype Annotations
Objects Annotated

Additional Information

CRRD Object Information
CRRD ID: 10003156
Created: 2015-05-05
Species: All species
Last Modified: 2015-05-05
Status: ACTIVE


RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.