Mutations in mitochondrial tRNA genes: non-linkage with syndromes of Wolfram and chronic progressive external ophthalmoplegia.

We have recently identified a point mutation in the mitochondrially encoded tRNA(Leu(UUR)) gene which associates with a combination of type II diabetes mellitus and sensorineural hearing loss in a large pedigree. To extend this finding to other syndromes which exhibit a combination of diabetes melli...

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Main Authors: van den Ouweland, J M, Bruining, G J, Lindhout, D, Wit, J M, Veldhuyzen, B F, Maassen, J A
Format: Artigo
Jezik:Inglês
Izdano: 1992
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC312004/
https://ncbi.nlm.nih.gov/pubmed/1542564
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