A novel mitochondrial DNA deletion in a patient with Kearns-Sayre syndrome: a late-onset of the fatal cardiac conduction deficit and cardiomyopathy accompanying long-term rGH treatment.

BMC pediatrics

Volumn 13, Issue , 2013, Pages

  Obara Moszynska, Monika ^a   Maceluch, Jaroslaw ^b   Bobkowski, Waldemar ^b   Baszko, Artur ^b   Jaremba, Oskar ^b   Krawczynski, Maciej R ^b   Niedziela, Marek ^b  

^a POZNAN UNIVERSITY OF MEDICAL SCIENCES   (Poland)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

HUMAN GROWTH HORMONE; MITOCHONDRIAL DNA; RECOMBINANT PROTEIN;

ADOLESCENT; ARTICLE; ATRIOVENTRICULAR BLOCK; CASE REPORT; CONGESTIVE CARDIOMYOPATHY; FATALITY; GENE DELETION; GENETICS; GROWTH DISORDER; HUMAN; KEARNS SAYRE SYNDROME; MALE; NUCLEOTIDE SEQUENCE;

ADOLESCENT; ATRIOVENTRICULAR BLOCK; BASE SEQUENCE; CARDIOMYOPATHY, DILATED; DNA, MITOCHONDRIAL; FATAL OUTCOME; GROWTH DISORDERS; HUMAN GROWTH HORMONE; HUMANS; KEARNS-SAYRE SYNDROME; MALE; RECOMBINANT PROTEINS; SEQUENCE DELETION;

MLCS; MLOWN;

EID: 84873975828     PISSN: None     EISSN: 14712431     Source Type: None    
DOI: 10.1186/1471-2431-13-27     Document Type: Article

References (0)