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Leigh, IM
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Citation: Na. Alam et al., Localization of a gene (MCUL1) for multiple cutaneous leiomyomata and uterine fibroids to chromosome 1q42.3-q43, AM J HU GEN, 68(5), 2001, pp. 1264-1269
Authors:
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Citation: R. Sudbrak et al., Hailey-Hailey disease is caused by mutations in ATP2C1 encoding a novel Ca2+ pump, HUM MOL GEN, 9(7), 2000, pp. 1131-1140
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Citation: N. Flanagan et al., Pleiotropic effects of the melanocortin 1 receptor (MC1R) gene on human pigmentation, HUM MOL GEN, 9(17), 2000, pp. 2531-2537
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Citation: Fjd. Smith et al., Novel keratin 16 mutations and protein expression studies in pachyonychia congenita type 1 and focal palmoplantar keratoderma, EXP DERMATO, 9(3), 2000, pp. 170-177
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Citation: Je. Tcheng et al., Novel dosing regimen of eptifibatide in planned coronary stent implantation (ESPRIT): a randomised, placebo-controlled trial, LANCET, 356(9247), 2000, pp. 2037-2044
Authors:
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Citation: Vl. Ruiz-perez et al., ATP2A2 mutations in Darier's disease: variant cutaneous phenotypes are associated with missense mutations, but neuropsychiatric features are independent of mutation class, HUM MOL GEN, 8(9), 1999, pp. 1621-1630
Authors:
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Citation: E. Healy et al., Factors produced by activated leukocytes alter renal epithelial cell differentiation, KIDNEY INT, 56(4), 1999, pp. 1266-1269
Authors:
Leonard, M
Ryan, MP
Watson, AJ
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Citation: M. Leonard et al., Role of MAP kinase pathways in mediating IL-6 production in human primary mesangial and proximal tubular cells, KIDNEY INT, 56(4), 1999, pp. 1366-1377
Authors:
Korge, BP
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Citation: Bp. Korge et al., Identification of novel mutations in basic hair keratins hHb1 and hHb6 in monilethrix: Implications for protein structure and clinical phenotype, J INVES DER, 113(4), 1999, pp. 607-612
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Rowan, A
Bataille, V
MacKie, R
Healy, E
Bicknell, D
Bodmer, W
Tomlinson, I
Citation: A. Rowan et al., Somatic mutations in the Peutz-Jegners (LKB1/STKII) gene in sporadic malignant melanomas, J INVES DER, 112(4), 1999, pp. 509-511