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. Author manuscript; available in PMC: 2014 Aug 1.
Published in final edited form as: Biochem Genet. 2013 Mar 17;51(0):524–529. doi: 10.1007/s10528-013-9583-z

Table 1.

GJB2 variations detected in deaf patients from Hazara, Pakistan

Patient ID cDNA Change Amino Acid Change Status Hearing Loss
SIHT-13 71G→A W24X Homozygous Profound
SIHT-28 104T→G I35S Homozygous Severe to profound
SIHT-63 35delG G12VfsX1 Homozygous Moderate to severe