Molecular analysis in a Turkish patient with severe form of Hurler Syndrome: Identification of a novel c.826_828del3 mutation.

Articles > Case Report · 2010

Authors: Sema KALKAN UÇAR, Mahmut ÇOKER, F Bertola, G Casati, Ruhsar Damla GÖKŞEN, Şükran DARCAN

Erciyes Tıp Dergisi ( Erciyes Medical Journal ), National Refreed University Journal, National, 2010, vol 32, pp 41-44

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