High proportions of mtDNA duplications in patients with Kearns-Sayre syndrome occur in the heart

American Journal of Medical Genetics

Volumn 71, Issue 4, 1997, Pages 443-452

  Fromenty, Bernard ^a,b   Carrozzo, Rosalba ^a   Shanske, Sara ^a   Schon, Eric A ^a,c  

^a The New York Presbyterian Hospital   (United States)

^b BEAUJON HOSPITAL   (France)

^c NONE   (United States)

Author keywords

DNA; KSS; Long PCR; Mitochondria; Mitochondrial disease; Polymerase chain reaction; Progressive external ophthalmoplegia

Indexed keywords

ARTICLE; CASE REPORT; CHILD; CLINICAL FEATURE; DNA DETERMINATION; FEMALE; GENE DELETION; HUMAN; KEARNS SAYRE SYNDROME; MITOSIS; OPHTHALMOPLEGIA; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SOUTHERN BLOTTING;

ADOLESCENT; ADULT; AUTOPSY; BASE SEQUENCE; DNA, MITOCHONDRIAL; FEMALE; HUMANS; KEARNS-SAYER SYNDROME; LEIGH DISEASE; MALE; MYOCARDIUM; ORGAN SPECIFICITY; POLYMERASE CHAIN REACTION; REPETITIVE SEQUENCES, NUCLEIC ACID; SEQUENCE DELETION;

EID: 0030752678     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19970905)71:4<443::AID-AJMG14>3.0.CO;2-G     Document Type: Article

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