Correlation between audiometric data and the 35delG mutation in ten patients

Brazilian Journal of Otorhinolaryngology

Volumn 73, Issue 6, 2007, Pages 777-783

  Piatto, Vânia Belintani ^a,b,d   Moreira, Otávio Augusto Vasques ^b,d   Da Silva, Magali Aparecida Orate Menezes ^a,d   Maniglia, José Victor ^a,d   Pereira, Márcio Coimbra ^a,d   Sartorato, Edi Lúcia ^c,d  

^a Speech and Hearing Therapy Division

^b FAMERP ^*  (Brazil)

^c UNIVERSITY OF CAMPINAS   (Brazil)

^d FACULDADE DE MEDICINA DE SÃO JOSÉ DO RIO PRETO   (Brazil)

Author keywords

35delg mutation; Audiometry; Hearing loss; Molecular analysis

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; AUDIOMETRY; CHILD; CLINICAL ARTICLE; CONNEXIN 26 GENE; CONTROLLED STUDY; CORRELATION ANALYSIS; CROSS-SECTIONAL STUDY; FEMALE; GENE; GENE DELETION; GENE MUTATION; GENOTYPE PHENOTYPE CORRELATION; HEARING LOSS; HETEROZYGOTE; HOMOZYGOTE; HUMAN; MALE; PERCEPTION DEAFNESS; PREVALENCE; RETROSPECTIVE STUDY; GENETICS; GENOTYPE; HOSPITALIZATION; MUTATION; PHENOTYPE; PRESCHOOL CHILD;

CONNEXIN 26; GAP JUNCTION PROTEIN;

ADOLESCENT; ADULT; AUDIOMETRY; CHILD; CHILD, PRESCHOOL; CONNEXINS; CROSS-SECTIONAL STUDIES; FEMALE; GENOTYPE; HEARING LOSS, SENSORINEURAL; HUMANS; MALE; MUTATION; PHENOTYPE; RETROSPECTIVE STUDIES; SEVERITY OF ILLNESS INDEX;

EID: 44949207732     PISSN: 18088694     EISSN: 18088686     Source Type: Journal    
DOI: 10.1016/s1808-8694(15)31174-5     Document Type: Article

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