No association between FCGR2A and FCGR3A polymorphisms in Guillain-Barré Syndrome in a Brazilian population
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文摘

Human FCGR polymorphisms associated with Guillain-Barré Syndrome is studied in a single ethnical population.

FCGR genotypes and allele frequencies were similar for Guillain Barré Syndrome patients and controls.

None of FCGR genotypes or alleles were associated with either mild or sever clinical presentation of Guillain-Barré Syndrome.

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