CNIC researchers find a possible treatment for one of the main symptoms of premature aging disease
HGPS is a rare genetic disease that affects one in every 4-8 million births. The disease is caused by a spontaneous mutation in one of the two copies (alleles) of the gene LMNA, which codes for lamin A, a protein important for the integrity and function of the envelope surrounding the cell nucleus. The mutation causes incorrect processing of the messenger RNA for lamin proteins, resulting in the synthesis of an anomalous protein, called progerin.
The new study, published in the leading cardiovascular research journal Circulation, identifies a possible treatment to block ...