Molecular elucidations of hutchinson-gilford progeria syndrome: A hope for managing horrors of premature aging in children
Hutchinson-Gilford progeria syndrome (or Progeria) is an exceptionally rare genetic disorder in children. It is caused by a rare point mutation in the lamin gene. It encodes lamin A protein, resulting in the de-shaping of nuclear membrane. This altered structure of the nuclear membrane renders the n...
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| Principais autores: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
University of Karachi
2020-05-01
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| Series: | Pakistan Journal of Pharmaceutical Sciences |
| Acceso en liña: | https://pjps.pk/single-article?id=cmrvmxq1s00618qyetpvakgbk |
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