TY - JOUR
T1 - Tuberous sclerosis
AU - Roach, E. S.
AU - Delgado, M. R.
PY - 1995
Y1 - 1995
N2 - Tuberous sclerosis complex is a disorder of cellular differentiation and proliferation that is inherited as an autosomal dominant trait with variable penetrance and a high spontaneous mutation rate. Lesions occur in the brain, skin, kidneys, heart, and other organs. Recent studies suggest genetic heterogeneity, with at least two gene loci on chromosomes 9, 16, and perhaps 11.
AB - Tuberous sclerosis complex is a disorder of cellular differentiation and proliferation that is inherited as an autosomal dominant trait with variable penetrance and a high spontaneous mutation rate. Lesions occur in the brain, skin, kidneys, heart, and other organs. Recent studies suggest genetic heterogeneity, with at least two gene loci on chromosomes 9, 16, and perhaps 11.
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U2 - 10.1016/s0733-8635(18)30118-9
DO - 10.1016/s0733-8635(18)30118-9
M3 - Review article
C2 - 7712641
AN - SCOPUS:0028888906
SN - 0733-8635
VL - 13
SP - 151
EP - 161
JO - Dermatologic Clinics
JF - Dermatologic Clinics
IS - 1
ER -