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Prevalence of mitochondrial 1555A-->G mutation in European children.
Bitner-Glindzicz M, Pembrey M, Duncan A, Heron J, Ring SM, Hall A, Rahman S. Bitner-Glindzicz M, et al. Among authors: pembrey m. N Engl J Med. 2009 Feb 5;360(6):640-2. doi: 10.1056/NEJMc0806396. N Engl J Med. 2009. PMID: 19196684 No abstract available.
Mapping of DFN2 to Xq22.
Tyson J, Bellman S, Newton V, Simpson P, Malcolm S, Pembrey ME, Bitner-Glindzicz M. Tyson J, et al. Among authors: pembrey me. Hum Mol Genet. 1996 Dec;5(12):2055-60. doi: 10.1093/hmg/5.12.2055. Hum Mol Genet. 1996. PMID: 8968763
IsK and KvLQT1: mutation in either of the two subunits of the slow component of the delayed rectifier potassium channel can cause Jervell and Lange-Nielsen syndrome.
Tyson J, Tranebjaerg L, Bellman S, Wren C, Taylor JF, Bathen J, Aslaksen B, Sørland SJ, Lund O, Malcolm S, Pembrey M, Bhattacharya S, Bitner-Glindzicz M. Tyson J, et al. Among authors: pembrey m. Hum Mol Genet. 1997 Nov;6(12):2179-85. doi: 10.1093/hmg/6.12.2179. Hum Mol Genet. 1997. PMID: 9328483
Thyroid peroxidase: evidence for disease gene exclusion in Pendred's syndrome.
Gausden E, Armour JA, Coyle B, Coffey R, Hochberg Z, Pembrey M, Britton KE, Grossman A, Reardon W, Trembath R. Gausden E, et al. Among authors: pembrey m. Clin Endocrinol (Oxf). 1996 Apr;44(4):441-6. doi: 10.1046/j.1365-2265.1996.714536.x. Clin Endocrinol (Oxf). 1996. PMID: 8706311
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