Related content

Mutations in the gene for connexin 26 (GJB2) that cause hearing loss have a dominant negative effect on connexin 30

By Marziano N.K.  

Human Molecular Genetics, Vol. 12, Iss. 8, 2003-04 ,pp. : 805-812

Oxford University Press

Access to resources Recommend Favorite

Properties of connexin26 gap junctional proteins derived from mutations associated with non-syndromal heriditary deafness

By Martin Patricia E.M.   L. Coleman Sharon   Casalotti Stefano O.   Forge Andy   Evans W. Howard  

Human Molecular Genetics, Vol. 8, Iss. 13, 1999-12 ,pp. : 2369-2376

Oxford University Press

Access to resources Recommend Favorite

Alterations in expression levels of deafness dystonia protein 1 affect mitochondrial morphology

By Engl Gertraud   Florian Stefan   Tranebjærg Lisbeth   Rapaport Doron  

Human Molecular Genetics, Vol. 21, Iss. 2, 2012-01 ,pp. : 287-299

Oxford University Press

Access to resources Recommend Favorite

Two Different Connexin 26 Mutations in an Inbred Kindred Segregating Non-Syndromic Recessive Deafness: Implications for Genetic Studies in Isolated Populations

By Carrasquillo Minerva M.   Zlotogora Joel   Barges Saleh   Chakravarti Aravinda  

Human Molecular Genetics, Vol. 6, Iss. 12, 1997-11 ,pp. : 2163-2172

Oxford University Press

Access to resources Recommend Favorite

Human Connexin 32, a gap junction protein altered in the X-linked form of Charcot–Marie–Tooth disease, is directly regulated by the transcription factor SOX10

By Dubourg O.   Bondurand N.   Girard M.   Pingault V.   Lemort N.   Goossens M.  

Human Molecular Genetics, Vol. 10, Iss. 24, 2001-11 ,pp. : 2783-2795

Oxford University Press

Access to resources Recommend Favorite