reference/14104422

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/14104422

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publicationName	Pediatric Pulmonology
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bibliographicCitation	Low KJ, Turnbull AR, Smith KR, Hilliard TN, Hole LJ, Meecham Jones DJ, Williams MM, Donaldson A. A case of congenital central hypoventilation syndrome in a three-generation family with non-polyalanine repeat PHOX2B mutation. Pediatr Pulmonol. 2014 Oct;49(10):E140–3. doi: 10.1002/ppul.23051. PMID: 24799442.
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date	2014-05-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://doi.org/10.1002/ppul.23051 https://pubmed.ncbi.nlm.nih.gov/24799442
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	A case of congenital central hypoventilation syndrome in a three‐generation family with non‐polyalanine repeat PHOX2B mutation
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Total number of triples: 49.