Title : Monomelic amyotrophy associated with the 7472insC mutation in the mtDNA tRNASer(UCN) gene.

Pub. Date : 2004 Nov

PMID : 15482956






1 Functional Relationships(s)
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1 The patient was found to have high levels of a known pathogenic mutation of mtDNA, the 7472insC in the gene encoding the tRNA(Ser(UCN)). Serine urocortin Homo sapiens