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Junctophilin 3 (JPH3) expansion mutations causing Huntington disease like 2 (HDL2) are common in South African patients with African ancestry and a Huntington disease phenotype.
Krause A, Mitchell C, Essop F, Tager S, Temlett J, Stevanin G, Ross C, Rudnicki D, Margolis R. Krause A, et al. Among authors: temlett j. Am J Med Genet B Neuropsychiatr Genet. 2015 Oct;168(7):573-85. doi: 10.1002/ajmg.b.32332. Epub 2015 Jun 16. Am J Med Genet B Neuropsychiatr Genet. 2015. PMID: 26079385 Free PMC article.
Pure word deafness.
Wolberg SC, Temlett JA, Fritz VU. Wolberg SC, et al. Among authors: temlett ja. S Afr Med J. 1990 Dec 1;78(11):668-70. S Afr Med J. 1990. PMID: 2251612
Polymyositis associated with Klinefelter's syndrome.
Nielsen SM, Rascher C, Temlett JA, Fritz VU. Nielsen SM, et al. Among authors: temlett ja. S Afr Med J. 1999 Apr;89(4):420-1. S Afr Med J. 1999. PMID: 10341830 No abstract available.
39 results