Recognition of mitochondrial DNA deletion syndrome with non-neuromuscular multisystemic manifestation

Genetics in Medicine

Volumn 3, Issue 6, 2001, Pages 399-404

  Wong, Lee Jun C ^a  

^a GEORGETOWN UNIVERSITY   (United States)

Author keywords

Kearns Sayre syndrome; mtDNA deletion; Pearson syndrome

Indexed keywords

MITOCHONDRIAL DNA;

ADOLESCENT; ADULT; ARTICLE; BLOOD SAMPLING; CHILD; CLINICAL FEATURE; CORRELATION ANALYSIS; DIAGNOSTIC PROCEDURE; DISORDERS OF MITOCHONDRIAL FUNCTIONS; DNA SEQUENCE; EXTERNAL OPHTHALMOPLEGIA; GENE DELETION; GENE LOCATION; GENE MUTATION; GENETIC ASSOCIATION; HUMAN; KEARNS SAYRE SYNDROME; MAJOR CLINICAL STUDY; MEDICAL LITERATURE; MITOCHONDRIAL MYOPATHY; MOLECULAR DYNAMICS; MUSCLE BIOPSY; NEUROMUSCULAR DISEASE; ONSET AGE; PEARSON SYNDROME; POLYMERASE CHAIN REACTION; POPULATION RISK; SOUTHERN BLOTTING; STATISTICAL ANALYSIS;

EID: 0035746672     PISSN: 10983600     EISSN: None     Source Type: Journal    
DOI: 10.1097/00125817-200111000-00004     Document Type: Article

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