A 1 bp deletion in the dual reading frame deafness gene LRTOMT causes a frameshift from the first into the second reading frame.

نویسندگان

  • Maarten Vanwesemael
  • Isabelle Schrauwen
  • Ruben Ceuppens
  • Fatemeh Alasti
  • Ellen Jorssen
  • Effat Farrokhi
  • Morteza Hashemzadeh Chaleshtori
  • Guy Van Camp
چکیده

A 1 bp Deletion in the Dual Reading Frame Deafness Gene LRTOMT Causes a Frameshift From the First Into the Second Reading Frame Maarten Vanwesemael, Isabelle Schrauwen, Ruben Ceuppens, Fatemeh Alasti, Ellen Jorssen, Effat Farrokhi, Morteza Hashemzadeh Chaleshtori, and Guy Van Camp* Department of Medical Genetics, University of Antwerp, 2610, Wilrijk, Belgium Cellular and Molecular Research Center, School of Medicine, Shahrekord University of Medical Sciences, Shahrekord, Iran

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عنوان ژورنال:
  • American journal of medical genetics. Part A

دوره 155A 8  شماره 

صفحات  -

تاریخ انتشار 2011