Author: Harhouri Karim Navarro Claire Baquerre Camille Da Silva Nathalie Bartoli Catherine Casey Frank Mawuse Guedenon Koffi Doubaj Yassamine Lévy Nicolas De Sandre-Giovannoli Annachiara
Publisher: MDPI
E-ISSN: 2073-4409|5|3|31-31
ISSN: 2073-4409
Source: Cells, Vol.5, Iss.3, 2016-07, pp. : 31-31
Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.
Abstract
Progeroid laminopathies, including Hutchinson-Gilford Progeria Syndrome (HGPS, OMIM #176670), are premature and accelerated aging diseases caused by defects in nuclear A-type Lamins. Most HGPS patients carry a de novo point mutation within exon 11 of the
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