Low prevalence of DFNB1 (connexin 26) mutations in British Pakistani children with non-syndromic sensorineural hearing loss

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Bibliographic Details
Main Author:	Yoong, s.Y
Other Authors:	ET AL
Format:	Journal Article
Language:	English
Subjects:	Anomalías genéticas Detección neonatal Discapacidad auditiva Estudio comparativo Minorías Reino Unido Discapacidad Documental
Online Access:	DOI Path
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