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CORRESPONDENCE: Sirolimus Therapy in Tuberous Sclerosis or Sporadic Lymphangioleiomyomatosis

. To the Editor: Tuberous sclerosis is an autosomal dominant disorder characterized by hamartomatous growths in many organs and caused by inherited mutations of the TSC1 or TSC2 gene. Acquired (somatic) mutations of either gene occur within ...

From DAVIES, D. M., JOHNSON, S. R., TATTERSFIELD, A. E., KINGSWOOD, J. C., COX, J. A., MCCARTNEY, D. L., DOYLE, T., ELMSLIE, F., SAGGAR, A., DE VRIES, P. J., SAMPSON, J. R., New England Journal of Medicine -- Recent Issues,  9 Jan 2008

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