Items where Author is "Olpin, SE"
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Alston, CL, Ceccatelli Berti, C, Blakely, EL, Olahova, M, He, L, McMahon, CJ, Olpin, SE, Hargreaves, IP, Nolli, C, McFarland, R, Goffrini, P, O'Sullivan, MJ and Taylor, RW (2015) A recessive homozygous p.Asp92Gly SDHD mutation causes prenatal cardiomyopathy and a severe mitochondrial complex II deficiency. Human Genetics, 134 (8). pp. 869-879. ISSN 0340-6717