Genetic and functional analyses of FH mutations in multiple cutaneous and uterine leiomyomatosis, hereditary leiomyomatosis and renal cancer, and fumarate hydratase deficiency

N A Alam, A J Rowan, N C Wortham, P J Pollard, M Mitchell, J P Tyrer, E Barclay, E Calonje, S Manek, S. J. Adams, P W Bowers, N P Burrows, R Charles-Holmes, L J Cook, B M Daly, G P Ford, L C Fuller, S E Hadfield-Jones, N Hardwick, A S HighetM Keefe, S P MacDonald-Hull, E D A Potts, M Crone, S Wilkinson, F Camacho-Martinez, S Jablonska, R Ratnavel, A MacDonald, R J Mann, K Grice, G Guillet, M. S. Lewis-Jones, H McGrath, D C Seukeran, P J Morrison, S Fleming, S Rahman, D Kelsell, I Leigh, S Olpin, I P M Tomlinson

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