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Novel LMNA Gene Mutation in a Patient With Atypical Werner's Syndrome
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 the severe metabolic complications, the extent...
| Autores principales: | , , , , , , |
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| Formato: | Texto |
| Lenguaje: | English |
| Publicado: |
The Korean Association of Internal Medicine
2009
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2687649/ https://www.ncbi.nlm.nih.gov/pubmed/19270485 http://dx.doi.org/10.3904/kjim.2009.24.1.68 |