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Characterisation of a novel TSC2 missense mutation in the GAP related domain associated with minimal clinical manifestations of tuberous sclerosis
- Correspondence to: Dr K Mayer Laboratory for Medical Genetics, Lochhamer Str. 29, 82152 Martinsried, Germany; mayermedizinische-genetik.de
Citation
Characterisation of a novel TSC2 missense mutation in the GAP related domain associated with minimal clinical manifestations of tuberous sclerosis
Publication history
- Accepted September 1, 2003
- Revised August 14, 2003
- First published April 30, 2004.
Online issue publication
April 27, 2016
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Copyright 2004 Journal of Medical Genetics