Chromosome 13

#	Item
21	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 Language: English Integral membrane proteins Connexin Deafness GJB2 Gap junction GJB6 Connexon GJB3 Chromosome 13 Biology Cell biology Genodermatoses
22	Hum Genet[removed] : 284–289 DOI[removed]s00439[removed] Add to Reading List Source URL: www.tau.ac.il Language: English - Date: 2010-11-12 08:57:39 Philosophy of biology Channelopathy Nonsyndromic deafness GJB2 Sensorineural hearing loss Connexin Chromosome 13 Mutation Haplotype Genetics Biology Deafness