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Association of a functional polymorphism of <i>PTPN22</i> encoding a lymphoid protein phosphatase in bilateral Meniere's disease

46

Citations

21

References

2009

Year

Abstract

These results suggest that the PTPN22 1858C/T genotype may confer differential susceptibility to BMD in the Spanish population and support an autoimmune etiology for BMD.

References

YearCitations

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