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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Detalhes bibliográficos
Main Authors: Doh, Yun Jeong, Kim, Hee Kyoung, Jung, Eui Dal, Choi, Seung Hee, Kim, Jung Guk, Kim, Bo Wan, Lee, In Kyu
Formato: Artigo
Idioma:Inglês
Publicado em: The Korean Association of Internal Medicine 2009
Assuntos:
Case Report
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2687649/
https://ncbi.nlm.nih.gov/pubmed/19270485
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3904/kjim.2009.24.1.68
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