Identification of a histone deacetylase inhibitor as a therapeutic candidate for congenital central hypoventilation syndrome
Congenital central hypoventilation syndrome (CCHS), a rare genetic disease caused by heterozygous PHOX2B mutations, is characterized by life-threatening breathing deficiencies. PHOX2B is a transcription factor required for the specification of the autonomic nervous system, which contains, in particu...
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Elsevier,
2024-12-01T00:00:00Z.
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A1234.567 |
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