Functional characterization of the TSC2 c.3598C > T (p.R1200W) missense mutation that co-segregates with tuberous sclerosis complex in mildly affected kindreds

M. Wentink, M. Nellist, M. Hoogeveen-Westerveld, B. Zonnenberg, D. van der Kolk, T. van Essen, S.M. Park, G. Woods, P.E. Hokke, W. Brussel, E. Smeets, A. Brooks, D. Halley, A. van den Ouweland, A. Maat-Kievit

Research output: Contribution to journalArticleAcademicpeer-review

Original languageUndefined/Unknown
Pages (from-to)453-461
JournalClinical Genetics
Issue number5
Publication statusPublished - 2012

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