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Nature, ISSN 0028-0836, 04/2009, Volume 458, Issue 7238, pp. 597 - 602
Journal Article
Journal Article
Connexin 26 and autosomal recessive non-syndromic hearing loss, 07/2003
Prelingual deafness occurs with a frequency of 1 in 1000 live births and is divided into syndromic and non-syndromic forms contributing 40 and 60%... 
hg03010 Non-syndromic, Hearing loss, Autosomal recessive, Connexin 26, DFNB1, mutation detection, Gap junction proteins, GJB2 | Genetics
Journal
Journal Article
Scientific Reports, ISSN 2045-2322, 12/2018, Volume 8, Issue 1, pp. 13975 - 11
Connexins are a family of membrane-spanning proteins named according to their molecular weight. They are known to form membrane channels mediating cell-cell... 
HEART | CELLS | H9C2 | CX26 | MULTIDISCIPLINARY SCIENCES | DISEASE | GENES | Heart | Deafness | Intercellular signalling | Phenotypes | Cardiomyocytes | Cell interactions | Membrane channels | Molecular weight | Connexin 26 | Skin diseases | Connexins | Localization | Cytoplasm
Journal Article
Journal Article
Human Genetics, ISSN 0340-6717, 10/2002, Volume 111, Issue 4, pp. 394 - 397
Mutations in GJB2, encoding gap junction beta 2 protein (connexin 26), are responsible for the commonest form of non-syndromic recessive deafness in many... 
NONSYNDROMIC HEARING-LOSS | CHILDHOOD DEAFNESS | FREQUENCY | GENETICS & HEREDITY | JAPANESE | GENE GJB2 | RECESSIVE DEAFNESS | IMPAIRMENT | Connexin 26 | Deafness - genetics | China | Humans | Alleles | Connexins - genetics | Deafness - ethnology | Female | Genotype | Male | Mutation | Index Medicus
Journal Article
Journal Article
Biochemical and Biophysical Research Communications, ISSN 0006-291X, 05/2014, Volume 448, Issue 1, pp. 28 - 32
Journal Article
Nature, ISSN 0028-0836, 05/1998, Volume 393, Issue 6683, pp. 319 - 320
A high proportion of all cases of congenital deafness is causedby mutations in a gene coding for a gap-junction protein,connexin 26. The deafness associated... 
MULTIDISCIPLINARY SCIENCES | Connexin 26 | Deafness - genetics | Genes, Dominant | DNA Mutational Analysis | Humans | Chromosomes, Human, Pair 13 | Connexins - genetics | Cysteine - chemistry | Mutation | Connexins - chemistry | Polymorphism, Genetic | Hearing | Genetic aspects | Research | Human genetics | Index Medicus
Journal Article
Journal Article
Biochemical and Biophysical Research Communications, ISSN 0006-291X, 10/2019, Volume 518, Issue 2, pp. 357 - 361
Connexin26 (Cx26) and Cx30 are the predominant connexin subtypes found in the cochlea. They play an essential role in the cochlear functions. However, most... 
Cochlea | Connexin | Guinea pig | Gap junction | Monkey | Index Medicus
Journal Article