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pro vyhledávání: '"Maria J. Eriksson"'
Publikováno v:
Aging Cell. 10:1011-1020
Hutchinson-Gilford progeria syndrome (HGPS or progeria) is a very rare genetic disorder with clinical features suggestive of premature aging. Here, we show that induced expression of the most common HGPS mutation (LMNA c.1824C>T, p.G608G) results in
Publikováno v:
PLoS ONE, Vol 4, Iss 1, p e4114 (2009)
PLoS ONE
PLoS ONE
Multiple genetic disorders caused by mutations that affect the proteins lamin A and C show strong skin phenotypes. These disorders include the premature aging disorders Hutchinson-Gilford progeria syndrome and mandibuloacral dysplasia, as well as res
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6ff26d66a7b9c15cf967cff6f11dd0d5
http://hdl.handle.net/10138/161764
http://hdl.handle.net/10138/161764