A Novel Homozygous Mutation in the EC1 EC2 Interaction Domain of the Gap Junction Complex Connexon 26 Leads to Profound Hearing Impairment - GJB6 - Document - PDFSEARCH.IO

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Integral membrane proteins Connexin Deafness GJB2 Gap junction GJB6 Connexon GJB3 Chromosome 13 Biology Cell biology Genodermatoses		A Novel Homozygous Mutation in the EC1/EC2 Interaction Domain of the Gap Junction Complex Connexon 26 Leads to Profound Hearing Impairment Add to Reading List Source URL: www.ncbi.nlm.nih.gov Download Document from Source Website File Size: 1,49 MB Share Document on Facebook

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	Gabriel et al. Head & Face Medicine 2012, 8(Suppl 1):O1 http://www.head-face-med.com/content/8/S1/O1 HEAD & FACE MEDICINE ORAL PRESENTATION DocID: 13m7w - View Document
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