bibliographic entry 8003937 [be/8003937]
https://w3id.org/oc/corpus/be/8003937
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Calvo SE, Tucker EJ, Compton AG, Kirby DM, Crawford G, Burtt NP, et al (2010) High-throughput, pooled sequencing identifies mutations in NUBPL and FOXRED1 in human complex I deficiency. Nat Genet 42: 851â858. doi: 10.1038/ng.659 PMID: 20818383
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