A novel mutation which causes a frameshift in the PHOX2B gene causes Haddad syndrome
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Date
Journal Title
Journal ISSN
Volume Title
Publisher
Lippincott Williams & Wilkins
Access Rights
info:eu-repo/semantics/closedAccess
Abstract
[Abstract Not Available]
Description
Keywords
Central Hypoventilation Syndrome, Phenotype, Children
Journal or Series
Clinical Dysmorphology
WoS Q Value
Scopus Q Value
Volume
29
Issue
3
