Detection of mitochondrial DNA mutations in patients with diabetes mellitus

Comment

A W Thomas et al. Diabetologia. 1995 Mar.

. 1995 Mar;38(3):376-7.

doi: 10.1007/BF00400645.

No abstract available

Comment on

Non-isotopic and sensitive method for diagnosis of maternally-inherited diabetes and deafness.
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Selection of primers for detection of A to G mutation at nucleotide 3243 of the mitochondrial gene.
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New sensitive method for the detection of the A3243G mutation of human mitochondrial deoxyribonucleic acid in diabetes mellitus patients by ligation-mediated polymerase chain reaction.
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[Detection and prevalence of mitochondrial genome mutations in diabetes].
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Diabetes mellitus is one of the heterogeneous phenotypic features of a mitochondrial DNA point mutation within the tRNALeu(UUR) gene.
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