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A case of congenital central hypoventilation syndrome in a three-generation family with non-polyalanine repeat PHOX2B mutation

✍ Scribed by Low, K.J.; Turnbull, A.R.; Smith, K.R.; Hilliard, T.N.; Hole, L.J.; Meecham Jones, D.J.; Williams, M.M.; Donaldson, A.

Book ID: 126166064
Publisher: John Wiley and Sons
Year: 2014
Tongue: English
Weight: 175 KB
Volume: 49
Category: Article
ISSN: 8755-6863
DOI: 10.1002/ppul.23051

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