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...
Tallennettuna:
| Päätekijät: | , , , , , |
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| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
University of Karachi
2020-05-01
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| Sarja: | Pakistan Journal of Pharmaceutical Sciences |
| Linkit: | https://pjps.pk/single-article?id=cmrvmxq1s00618qyetpvakgbk |
| Tagit: |
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