(Q35445725)
Statements
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Characterisation of a novel TSC2 missense mutation in the GAP related domain associated with minimal clinical manifestations of tuberous sclerosis (English)
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Mayer K
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Goedbloed M
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van Zijl K
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Nellist M
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Rott HD
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1 May 2004
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41
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5
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e64
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Identifiers
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