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...

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Detalles Bibliográficos
Autores principales: Doh, Yun Jeong, Kim, Hee Kyoung, Jung, Eui Dal, Choi, Seung Hee, Kim, Jung Guk, Kim, Bo Wan, Lee, In Kyu
Formato: Texto
Lenguaje:English
Publicado: The Korean Association of Internal Medicine 2009
Materias:
Case Report
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

Internet

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

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