Dyfyniad APA

Calvo, S. E., Tucker, E. J., Compton, A. G., Kirby, D. M., Crawford, G., Burtt, N. P., . . . Mootha, V. K. (2010). High-throughput, pooled sequencing identifies mutations in NUBPL and FOXRED1 in human complex I deficiency.

Dyfyniad Arddull Chicago

Calvo, Sarah E., et al. High-throughput, Pooled Sequencing Identifies Mutations in NUBPL and FOXRED1 in Human Complex I Deficiency. 2010.

Dyfyniad MLA

Calvo, Sarah E., et al. High-throughput, Pooled Sequencing Identifies Mutations in NUBPL and FOXRED1 in Human Complex I Deficiency. 2010.

Rhybudd: Mae'n bosib nad yw'r dyfyniadau hyn bob amser yn 100% cywir.