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Congenital central hypoventilation syndrome with PHOX2B gene mutation: are we missing the diagnosis?
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Congenital central hypoventilation syndrome with PHOX2B gene mutation: are we missing the diagnosis?
Congenital central hypoventilation syndrome with PHOX2B gene mutation: are we missing the diagnosis? Indian J Pediatr. 2013 Aug; 80(8):688-90.
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PubMed
subject areas
Chromosomes, Human, Pair 4
DNA Repeat Expansion
Female
Homeodomain Proteins
Humans
Hypoventilation
Infant, Newborn
Sleep Apnea, Central
Transcription Factors
authors with profiles
Elizabeth Berry-Kravis