2 studies found for:
PHOX2B
| Rank | Status | Study | ||||
|---|---|---|---|---|---|---|
| 1 | Recruiting |
PHOX2B Mutation-Confirmed Congenital Central Hypoventilation Syndrome in A Chinese Family: Presentations From Newborn to Adulthood
|
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| 2 | Completed |
Late-onset Congenital Central Hypoventilation Syndrome and the Mutation of Phox2B Gene
|
† Indicates status has not been verified in more than two years