Clinical Trial Update: Late-onset Congenital Central Hypoventilation Syndrome and the Mutation of Phox2B Gene

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Summary

A completed clinical trial update examining late-onset congenital central hypoventilation syndrome and its association with Phox2B gene mutation.

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Diseases / indications

• Congenital Central Hypoventilation Syndrome

Snippet

Sponsor: Associação Fundo de Incentivo à Pesquisa | Conditions: Congenital Central Hypoventilation Syndrome | Status: COMPLETED