Increased Prevalence of Familial Autoimmunity in Probands With Pervasive Developmental Disorders
Author:
Affiliation:
1. Departments of Psychiatry
2. Pediatrics, Indiana University School of Medicine, and James Whitcomb Riley Hospital for Children Indianapolis, Indiana
3. St Vincent Hospital, Indianapolis, Indiana
Abstract
Publisher
American Academy of Pediatrics (AAP)
Subject
Pediatrics, Perinatology, and Child Health
Link
https://publications.aap.org/pediatrics/article-pdf/112/5/e420/1002853/pe110300e420.pdf
Reference35 articles.
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3. Fielder AH, Walport MJ, Batchelor JR, et al. Family study of the major histocompatibility complex in patients with systemic lupus erythematosus: importance of null alleles of C4A and C4B in determining disease susceptibility. Br Med J.1983;286:425–428
4. Warren RP, Singh VK, Cole P, et al. Increased frequency of the null allele at the complement C4b locus in autism. Clin Exp Immunol.1991;83:438–440
5. Warren RP, Singh VK, Cole P, et al. Possible association of the extended MHC haplotype B44-SC30-DR4 with autism. Immunogenetics.1992;36:203–207
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