Phenotypic heterogeneity in British patients with a founder mutation in the FHL1 gene. by Sarkozy, A, Windpassinger, C, Hudson, J, Dougan, C, Lecky, B, Hilton-Jones, D, Eagle, M, Charlton, R, Barresi, R, Lochmüller, H, Bushby, K, Straub, V

Pathogenic mtDNA mutations causing mitochondrial myopathy: the need for muscle biopsy by Hardy, S, Blakely, E, Purvis, A, Rocha, M, Ahmed, S, Falkous, G, Poulton, J, Rose, M, O'Mahony, O, Bermingham, N, Dougan, C, Ng, Y, Horvath, R, Turnbull, D, Gorman, G, Taylor, R