A case of a de novo A3243G mutation in mitochondrial DNA in a patient with diabetes and deafness.

Maassen, J A

A case of a de novo A3243G mutation in mitochondrial DNA in a patient with diabetes and deafness. [electronic resource] - Archives of physiology and biochemistry Jul 2002 - 186-8 p. digital

Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't

1381-3455

10.1076/apab.110.3.186.8294 doi


Adult
DNA, Mitochondrial
Deafness--genetics
Diabetes Mellitus--genetics
Female
Heterozygote
Humans
Male
Middle Aged
Mutation
Syndrome