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2 studies found for:    PHOX2B
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PHOX2B (2 records)
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Rank Status Study
1 Unknown  PHOX2B Mutation-Confirmed Congenital Central Hypoventilation Syndrome in A Chinese Family: Presentations From Newborn to Adulthood
Condition: Central Alveolar Hypoventilation Syndrome
Intervention: Device: CPAP
2 Completed Late-onset Congenital Central Hypoventilation Syndrome and the Mutation of Phox2B Gene
Condition: Congenital Central Hypoventilation Syndrome
Intervention: Device: positive airway pressure, Non-invasive mechanic ventilation

Indicates status has not been verified in more than two years