Distinct clustering of point mutations in mitochondrial DNA among patients with mitochondrial encephalomyopathies and with Parkinson's disease

Biochemical and Biophysical Research Communications

Volumn 176, Issue 2, 1991, Pages 938-946

  Ozawa, Takayuki ^a,d,e   Tanaka, Masashi ^a,d,e   Ino, Hidekazu ^a,d,e   Ohno, Kinji ^a,d,e   Sano, Tadashi ^b,d,e   Wada, Yoshiro ^b,d,e   Yoneda, Makoto ^b,d,e   Tanno, Yoshinori ^b,d,e   Miyatake, Tadashi ^b,d,e   Tanaka, Taihei ^d,e   Itoyama, Shinji ^b,d,e   Ikebe, Shin ichiro ^c,d,e   Hattori, Nobutaka ^c,d,e   Mizuno, Yoshikuni ^c,d,e  

^a NAGOYA UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^b NAGOYA CITY UNIV MEDICAL SCHOOL   (Japan)

^c NIIGATA UNIVERSITY   (Japan)

^d SAITAMA MEDICAL UNIVERSITY   (Japan)

^e JUNTENDO UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

MITOCHONDRIAL DNA;

ADULT; AGED; ARTICLE; AUTOPSY; CLINICAL ARTICLE; FEMALE; HUMAN; HUMAN TISSUE; MALE; MYOPATHY; PARKINSON DISEASE; POINT MUTATION; PRIORITY JOURNAL;

ADOLESCENT; ADULT; DNA, MITOCHONDRIAL; FEMALE; HUMAN; MALE; MIDDLE AGE; MITOCHONDRIA, MUSCLE; MULTIGENE FAMILY; MUTATION; PARKINSON DISEASE; PHYLOGENY; SUPPORT, NON-U.S. GOV'T;

EID: 0025863393     PISSN: 0006291X     EISSN: 10902104     Source Type: Journal    
DOI: 10.1016/S0006-291X(05)80276-1     Document Type: Article

References (30)

1. The complete nucleotide sequence of theRattus norvegicus mitochondrial genome: Cryptic signals revealed by comparative analysis between vertebrates