conexina 26

Es un subtipo de conexina codificada en el cromosoma 13q11-12. La mutación autosómica recesiva del gen que la codifica es la causa más frecuente de pérdida de audición congénita no sindrómica.

Diccionario de términos sencillos BioDic

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© Centro de Investigación y Desarrollo de Recursos Científicos BioScripts.
BioDic – Diccionario de Biología – Un diccionario de términos científicos, sencillo.

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