Exome sequencing identifies NFS1 deficiency in a novel Fe-S cluster disease, infantile mitochondrial complex II/III deficiency.

Mol Genet Genomic Med · 2014 · PMC3907916 · PMID 24498631

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closest p

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highly significantno p-value reported

Genome-wide autozygosity mapping generated a locus on chromosome 20p11.2-q13.1, ∼27.7 Mb with a highly significant location score of 1754 (Fig. 2 B).

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