4Cuevas SA, Jimenez AL, Gonzalez LM. Somatic and germinal mosaicism for the steroid sulfatase gene deletion in a steroid sulfatase deficiency carrier[J]. J Invest Dermatol, 2002, 119(4): 972-5.
5Gonzalez LM, Riviera MR, Kofman SH. Novel missense mutation(Arg432Cys) in a patient with steroid sulphatase-deficiency[J]. Clin Endocrinol (Oxf), 2003, 59(2): 263-4.
6Jimenez AL, Valdes Mdel R, Rivera MR. Deletion pattern of the STS gene in X-linked ichthyosis in a Mexican population [J]. Mol Med, 2001, 7(12): 845-9.
7Lesca G, Sinilnikova OM, Theuil G, et al. Xp22.3 microdeletion including VCX-A and VCX-B1 genes in an X-linked ichthyosis family: no difference in deletion size for patients with and without mental retardation[J]. Clin Genetics, 2005, 67(4): 367.
9Valdes M, Kofman SH, Vaca AL, et al. Mutation report: a novel partial deletion of exons 2-10 of the STS gene in recessive X-linked ichthyosis[J]. J Invest Dermatol, 2000, 114(3): 591-3.
10Hernandez A, Gonzalez R, De Unamuno P. X-linked ichthyosis: an update[J]. Br J Demerol, 1999, 141(4): 617-27.