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Publikováno v:
Biochemical Society Transactions. 36:1389-1392
The laminopathy Hutchinson–Gilford progeria syndrome (HGPS) is caused by the mutant lamin A protein progerin and leads to premature aging of affected children. Despite numerous cell biological and biochemical insights into the basis for the cellula
Publikováno v:
Biochemical Society Transactions; 2008, Vol. 36 Issue 6, p1389-1392, 4p