Article
Recurrent mutation 4882delTT in the GAP-related domain of the tuberous sclerosis TSC2 gene.
Human mutation - 1 Jan 1998
Verhoef S, Vrtel R, Bakker L, Stolte-Dijkstra I, Nellist M, Begeer J H, Zaremba J, Jozwiak S, Tempelaars A M, Lindhout D, Halley D J, van den Ouweland A M
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