- Hutchinson-Gilford Progeria Syndrome with G608G LMNA Mutation
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Kim HK, Lee JY, Bae EJ, Oh PS, Park WI, Lee DS, Kim JI, Lee HJ
- KMID: 1786024
- J Korean Med Sci.
- 2011 Dec;26(12):1642-1645.
- doi: 10.3346/jkms.2011.26.12.1642
Hutchinson-Gilford progeria syndrome (HGPS) is a rare condition originally described by Hutchinson in 1886. Death result from cardiac complications in the majority of cases and usually occurs at average age... -
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