Concepedia

Publication | Open Access

Molecular Basis of DFNB73: Mutations of BSND Can Cause Nonsyndromic Deafness or Bartter Syndrome

DOIFull Paper Access

86

Citations

21

References

2009

Year

Saima Riazuddin, Saima Anwar, Martin Fischer, Zubair M. Ahmed, Shahid Y. Khan, Audrey G.H. Janssen, Ahmad Usman Zafar, Ute I. Scholl, Tayyab Husnaın, Inna A. Belyantseva,
The American Journal of Human Genetics

References

YearCitations

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