Did the GJB2 35delG mutation originate in Iran?

By  

American Journal Of Medical Genetics Part A, Vol. 155, Iss. 10, 2011-10 ,pp. : 2453-2458

John Wiley & Sons Inc

Access to resources Recommend Favorite

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

A missense mutation in connexin26, D66H, causes mutilating keratoderma with sensorineural deafness (Vohwinkel’s syndrome) in three unrelated families

By Maestrini Elena  

Human Molecular Genetics, Vol. 8, Iss. 7, 1999-07 ,pp. : 1237-1243

Oxford University Press

Access to resources Recommend Favorite

The human deafness-associated connexin 30 T5M mutation causes mild hearing loss and reduces biochemical coupling among cochlear non-sensory cells in knock-in mice

By Schtz Melanie   Scimemi Pietro   Majumder Paromita   De Siati Romolo Daniele   Crispino Giulia   Rodriguez Laura   Bortolozzi Mario   Santarelli Rosamaria   Seydel Anke   Sonntag Stephan   Ingham Neil   Steel Karen P.   Willecke Klaus   Mammano Fabio  

Human Molecular Genetics, Vol. 19, Iss. 24, 2010-12 ,pp. : 4759-4773

Oxford University Press

Access to resources Recommend Favorite

Pathogenetic role of the deafness-related M34T mutation of Cx26

By Bicego Massimiliano   Beltramello Martina   Carella Massimo   Piazza Valeria   Zelante Leopoldo   Bukauskas Feliksas F.   Arslan Edoardo   Cama Elona   Pantano Sergio   Bruzzone Roberto  

Human Molecular Genetics, Vol. 15, Iss. 17, 2006-09 ,pp. : 2569-2587

Oxford University Press

Access to resources Recommend Favorite