Frequency of mtDNA A1555G and A7445G mutations among children with prelingual deafness in Turkey

European Journal of Pediatrics

Volumn 162, Issue 3, 2003, Pages 154-158

  Tekin, M ^a,d   Duman, T ^a   Bogoclu G ^a   Incesulu, A ^b   Comak E ^c   Fitoz, S ^a   Yilmaz, E ^a   IIhan, I ^c   Akar, N ^a  

^a ANKARA UNIVERSITY   (Turkey)

^b Social Security Hospital   (Turkey)

^c SULEYMAN DEMIREL UNIVERSITY SCHOOL OF MEDICINE   (Turkey)

^d NONE   (Turkey)

Author keywords

Aminoglycoside toxicity; Cerebral infarct; Deafness; Mitochondrial mutations; Turkish population

Indexed keywords

AMINOGLYCOSIDE ANTIBIOTIC AGENT; CONNEXIN 26;

ADOLESCENT; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; BRAIN INFARCTION; CASE REPORT; CHILD; FEMALE; GENE FREQUENCY; GENE MUTATION; GENETIC ANALYSIS; GENETIC RISK; GENETIC SCREENING; HETEROZYGOTE; HUMAN; MALE; PARIETAL LOBE; PERCEPTION DEAFNESS; POPULATION GENETICS; PREVALENCE; PRIORITY JOURNAL;

EID: 0037340257     PISSN: 03406199     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00431-002-1129-z     Document Type: Article

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