A common mitochondrial DNA variant associated with susceptibility to dilated cardiomyopathy in two different populations

Lancet

Volumn 357, Issue 9264, 2001, Pages 1265-1267

  Khogali, Saib S ^a   Mayosi, Bongani M ^a   Beattie, James M ^b   McKenna, William J ^c   Watkins, Hugh ^a   Poulton, Joanna ^a  

^a UNIVERSITY OF OXFORD   (United Kingdom)

^b BIRMINGHAM HEARTLANDS HOSPITAL   (United Kingdom)

^c ST GEORGE S HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

MITOCHONDRIAL DNA;

ADULT; AGED; ARTICLE; CONTROLLED STUDY; DISEASE PREDISPOSITION; DNA POLYMORPHISM; FEMALE; HEART DILATATION; HUMAN; MAJOR CLINICAL STUDY; MALE; NON INSULIN DEPENDENT DIABETES MELLITUS; PRIORITY JOURNAL;

EID: 0035925906     PISSN: 01406736     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0140-6736(00)04422-6     Document Type: Article

References (5)

1. The frequency of dilated cardiomyopathy in a series of patients with idiopathic dilated cardiomyopathy
2. A common mitochondrial DNA variant is associated with insulin resistance in adult life
3. Mitochondrial 16189 variant, thinness at birth, and type 2 diabetes
4. Length heteroplasmy in the first hypervariable segment of the human mitochondrial DNA control region
5. Interpretation of results from genetic studies of multifactorial disease