Huntington Gilford Progeria Syndrome, HGPS

 

 

 

Gene

LMNA

OMIM Number

176670

Published DNA change

c.1824C>T

Proper Nomenclature

c.1824C>T

Published AA change

p.G608Gly

Proper Nomenclature

p.G608Gly

Number of chromosomes

2

Frequency %

Unknown

Source

Doubaj Y et al. Arch Pediatr. 2011;18:156-9