[The results of audiological examination of children presenting with sensorineural loss of hearing due to GJB2 gene mutations during the first year of life].

Vestnik otorinolaringologii

Volumn , Issue 3, 2011, Pages 31-35

  Lalaiants, M R ^a   Bliznets, E A ^a   Markova, T G ^a   Poliakov, A V ^a   Tavartkiladze, G A ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

CONNEXIN 26; DNA; GAP JUNCTION PROTEIN;

ARTICLE; AUDIOMETRY; COMPARATIVE STUDY; DISEASE COURSE; GENE FREQUENCY; GENETICS; GENOTYPE; HEARING LOSS; HUMAN; INFANT; METHODOLOGY; MUTATION; NEWBORN; NEWBORN SCREENING; NUCLEOTIDE SEQUENCE; PERCEPTION DEAFNESS;

AUDIOMETRY; CONNEXINS; DISEASE PROGRESSION; DNA; DNA MUTATIONAL ANALYSIS; GENE FREQUENCY; GENOTYPE; HEARING LOSS, BILATERAL; HEARING LOSS, SENSORINEURAL; HUMANS; INFANT; INFANT, NEWBORN; MUTATION; NEONATAL SCREENING;

EID: 80052644000     PISSN: 00424668     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (0)