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Autosomal codominant inheritance and Japanese incidence of deficiency of OKT4 epitope with lack of reactivity resulting from conformational change.
Takenaka T, Kuribayashi K, Nakamine H, Yoshikawa F, Maeda J, Kishi S, Nakauchi H, Minatogawa Y, Kido R. Takenaka T, et al. J Immunol. 1993 Sep 1;151(5):2864-70. J Immunol. 1993. PMID: 7689618
A large Japanese family in which some members were homozygous or heterozygous for OKT4 epitope deficiency was studied. Homozygotes, heterozygotes, and normal individuals were identified by differences in the number of OKT4 epitopes on the surfaces of lymphocy …
A large Japanese family in which some members were homozygous or heterozygous for OKT4 epitope deficiency was studied. …
Primary Sjogren's syndrome and psoriasis vulgaris in a case of OKT4 epitope deficiency.
Tanaka H, Mizutani H, Okada H, Shimizu M. Tanaka H, et al. J Dermatol. 1995 Apr;22(4):262-6. doi: 10.1111/j.1346-8138.1995.tb03383.x. J Dermatol. 1995. PMID: 7541811
We report a 29-year-old female OKT4 epitope deficiency patient with primary Sjogren's syndrome and psoriasis vulgaris. Immunological investigations during the prolonged clinical course of her herpes zoster revealed that she has OKT4 epitope …
We report a 29-year-old female OKT4 epitope deficiency patient with primary Sjogren's syndrome and psoriasis vulgaris. …