- Novel LMNA Gene Mutation in a Patient With Atypical Werner's Syndrome
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Doh YJ, Kim HK, Jung ED, Choi SH, Kim JG, Kim BW, Lee IK
- KMID: 1785645
- Korean J Intern Med.
- 2009 Mar;24(1):68-72.
- doi: 10.3904/kjim.2009.24.1.68
Hutchinson-Gilford progeria syndrome (HGPS) and Werner's syndrome are representative types of progeroid syndrome. LMNA (Lamin A/C) gene mutation with atypical Werner's syndrome have recently been reported. Atypical Werner's syndrome with... -
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- 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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