Patients with idiopathic cardiomyopathy belong to the same mitochondrial DNA gene family of Parkinson's disease and mitochondrial encephalomyopathy

Biochemical and Biophysical Research Communications

Volumn 177, Issue 1, 1991, Pages 518-525

  Ozawa, Takayuki ^a   Tanaka, Masashi ^a   Sugiyama, Satoru ^a   Ino, Hidekazu ^a   Ohno, Kinji ^a   Hattori, Kazuki ^a   Ohbayashi, Toshihiro ^a   Ito, Takayuki ^a   Deguchi, Hirofumi ^b   Kawamura, Keishiro ^b   Nakane, Yumiko ^c   Hashiba, Kunitake ^c  

^a NAGOYA UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^b OSAKA MEDICAL COLLEGE   (Japan)

^c NAGASAKI UNIVERSITY SCHOOL OF MEDICINE   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CARDIOMYOPATHY; CASE REPORT; DNA SEQUENCE; ENCEPHALOMYOPATHY; HEART; HUMAN; HUMAN TISSUE; IDIOPATHIC DISEASE; MITOCHONDRION; MUTATION; PARKINSON DISEASE; PRIORITY JOURNAL;

ADULT; BASE SEQUENCE; CARDIOMYOPATHY, HYPERTROPHIC; CASE REPORT; CENTRAL NERVOUS SYSTEM DISEASES; COMPARATIVE STUDY; DNA, MITOCHONDRIAL; ELECTROCARDIOGRAPHY; FEMALE; HUMAN; MALE; MITOCHONDRIA, MUSCLE; MOLECULAR SEQUENCE DATA; MULTIGENE FAMILY; MUTATION; MYOCARDIAL DISEASES; MYOCARDIUM; NUCLEIC ACID CONFORMATION; PARKINSON DISEASE; PEDIGREE; SUPPORT, NON-U.S. GOV'T;

EID: 0025915472     PISSN: 0006291X     EISSN: 10902104     Source Type: Journal    
DOI: 10.1016/0006-291X(91)92014-B     Document Type: Article

References (15)

1. Increase of deleted mitochondrial DNA in the striatum in Parkinson's disease and senescence
2. Multiple mitochondrial DNA deletions exist in cardiomyocytes of patients with hypertrophic or dilated cardiomyopathy
3. Sequence and properties of the human KB cell and mouse L cell D-loop regions of mitochondrial DNA