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PROGERIA IN SIBLINGS: A RARE CASE REPORT
Progeria, also known as Hutchinson-Gilford syndrome, is an extremely rare, severe genetic condition wherein symptoms resembling aspects of aging are manifested at an early age. It is an autosomal dominant disorder. It is not seen in siblings of affected children although there are very few case repo...
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| Main Authors: | , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Medknow Publications & Media Pvt Ltd
2011
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3221230/ https://ncbi.nlm.nih.gov/pubmed/22121285 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0019-5154.87162 |
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