Understanding the Complexities of Hyper Igm Syndrome
Hyper IgM Syndrome is a very rare disease caused by mutations in a gene located in the X chromosome. It affects approximately 1 in 1,000,000 individuals globally.
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Hyper IgM Syndrome is a very rare disease caused by mutations in a gene located in the X chromosome. It affects approximately 1 in 1,000,000 individuals globally.
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