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