Gap junctions and connexin expression in the inner ear

A Forge, D Becker, S Casalotti… - … 219‐Gap Junction …, 2007 - Wiley Online Library
Several different recessive mutations in the connexin26 (Cx26; β2) gene have been
associated with non‐syndromic hereditary deafness. This suggests gap junctions are …
被引用次数：140 相关文章

Gap junctions and connexin expression in the inner ear.

A Forge, D Becker, S Casalotti, J Edwards… - Novartis Foundation …, 1999 - europepmc.org
Several different recessive mutations in the connexin26 (Cx26; beta 2) gene have been
associated with non-syndromic hereditary deafness. This suggests gap junctions are …

Gap junctions and connexin expression in the inner ear

A Forge, D Becker, S Casalotti… - Novartis …, 1999 - pubmed.ncbi.nlm.nih.gov
Several different recessive mutations in the connexin26 (Cx26; beta 2) gene have been
associated with non-syndromic hereditary deafness. This suggests gap junctions are …

Gap junctions and connexin expression in the inner ear

A Forge, D Becker, S Casalotti, J Edwards… - Novartis Foundation …, 2007 - orca.cardiff.ac.uk
Several different recessive mutations in the connexin26 (Cx26; β2) gene have been
associated with non-syndromic hereditary deafness. This suggests gap junctions are …

[引用][C] Gap junctions and connexin expression in the inner ear

A FORGE - Novartis Found Symp, 1999 - cir.nii.ac.jp

Gap junctions and connexin expression in the inner ear

M Souter - Gap Junction-Mediated Intercellular Signalling in …, 2008 - books.google.com
Ahrtratt. Several different recessive mutations in the connexin26 (Cx26; B2) gene have been
associated with non-syndromic hereditary deafness. This suggests gap junctions are …

Gap junctions and connexin expression in the inner ear

A Forge - GAP JUNCTION-MEDIATED INTERCELLULAR …, 1999 - Wiley Online Library
Several different recessive mutations in the connexin26 (Cx26; &) gene have been
associated with non-syndromic hereditary deafness. This suggests gap junctions are …

Gap junctions and connexin expression in the inner ear

A Forge, D Becker, S Casalotti, J Edwards… - Novartis Foundation …, 2007 - orca.cardiff.ac.uk
Several different recessive mutations in the connexin26 (Cx26; β2) gene have been
associated with non-syndromic hereditary deafness. This suggests gap junctions are …