Huntington Gilford Progeria Syndrome, HGPS
Gene
LMNA
OMIM Number
176670
Published DNA change
c.1824C>T
Proper Nomenclature
Published AA change
p.G608Gly
Number of chromosomes
2
Frequency %
Unknown
Source
Doubaj Y et al. Arch Pediatr. 2011;18:156-9