Connexin 26 preverbal hearing impairment: Mutation prevalence and heterozygosity in a selected population: Problemas auditivos preverbales por Conexina 26: Prevalencia de mutacion y heterocigosidad en una población seleccionada
Autor: | Eva Orzan, Alberto Mazza, Alessandra Murgia, Franco Zacchello, Gregorio Babighian, Roberta Polli, Maddalena Martella |
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Rok vydání: | 2002 |
Předmět: |
Linguistics and Language
medicine.medical_specialty education.field_of_study business.industry Hearing loss Population Connexin Sensorineural hearing impairment Audiology Language and Linguistics Molecular analysis Loss of heterozygosity Speech and Hearing Mutation (genetic algorithm) otorhinolaryngologic diseases Medicine medicine.symptom Family history business education |
Zdroj: | International Journal of Audiology. 41:120-124 |
ISSN: | 1708-8186 1499-2027 |
DOI: | 10.3109/14992020209090402 |
Popis: | The objective of this investigation was to determine the prevalence of Cx26 mutations in familial and sporadic cases of non-syndromic preverbal hearing impairment (HI). Molecular analysis of the Co... |
Databáze: | OpenAIRE |
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