SLC26A4 mutation spectrum associated with DFNB4 deafness and Pendred's syndrome in Pakistanis - Concepedia

Concepedia

Publication | Open Access

SLC26A4 mutation spectrum associated with DFNB4 deafness and Pendred's syndrome in Pakistanis

DOI Full Paper Access

98

Citations

28

References

2009

Year

Saima Anwar, Saima Riazuddin, Zubair M. Ahmed, Saba Tasneem, Ateeq-ul-Jaleel, Shahid Y. Khan, Andrew J. Griffith, Thomas B. Friedman, Sheikh Riazuddin

Journal of Human Genetics

Mendelian DisorderGenetic DisorderGeneticsPathologySlc26a4 Mutation SpectrumDfnb4 DeafnessDisease Gene IdentificationMedicineVariant InterpretationClinical Genetics

References

	Year	Citations

Page 1

Page 1