APA

Alston C. L., Ceccatelli Berti C., Blakely E. L., Oláhová M., He L., McMahon C. J., Olpin S. E., Hargreaves I. P., Nolli C., McFarland R., Goffrini P., O'Sullivan M. J. & Taylor R. W. (20150918). A recessive homozygous p.Asp92Gly SDHD mutation causes prenatal cardiomyopathy and a severe mitochondrial complex II deficiency. : Human genetics.

Chicago

Alston Charlotte L, Ceccatelli Berti Camilla, Blakely Emma L, Oláhová Monika, He Langping, McMahon Colin J, Olpin Simon E, Hargreaves Iain P, Nolli Cecilia, McFarland Robert, Goffrini Paola, O'Sullivan Maureen J and Taylor Robert W. 20150918. A recessive homozygous p.Asp92Gly SDHD mutation causes prenatal cardiomyopathy and a severe mitochondrial complex II deficiency. : Human genetics.

Harvard

Alston C. L., Ceccatelli Berti C., Blakely E. L., Oláhová M., He L., McMahon C. J., Olpin S. E., Hargreaves I. P., Nolli C., McFarland R., Goffrini P., O'Sullivan M. J. and Taylor R. W. (20150918). A recessive homozygous p.Asp92Gly SDHD mutation causes prenatal cardiomyopathy and a severe mitochondrial complex II deficiency. : Human genetics.

MLA

Alston Charlotte L, Ceccatelli Berti Camilla, Blakely Emma L, Oláhová Monika, He Langping, McMahon Colin J, Olpin Simon E, Hargreaves Iain P, Nolli Cecilia, McFarland Robert, Goffrini Paola, O'Sullivan Maureen J and Taylor Robert W. A recessive homozygous p.Asp92Gly SDHD mutation causes prenatal cardiomyopathy and a severe mitochondrial complex II deficiency. : Human genetics. 20150918.