Concepedia

Publication | Open Access

Mutations of human <i>TMHS</i> cause recessively inherited non-syndromic hearing loss

DOIFull Paper Access

100

Citations

23

References

2006

Year

Muhammad Imran Shabbir, Zubair M. Ahmed, Shahid Y. Khan, Saima Riazuddin, Ali Muhammad Waryah, Shaheen N. Khan, Reyna D Camps, Manju Ghosh, Madulika Kabra, Inna A. Belyantseva,
Journal of Medical Genetics

Abstract

These findings establish the importance of TMHS for normal sound transduction in humans.

References

YearCitations

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