Delayed diagnosis of a patient with Usher syndrome 1C in a Louisiana Acadian family highlights the necessity of timely genetic testing for the diagnosis and management of congenital hearing loss

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Bibliographic Details
Published inSAGE open medical case reports Vol. 5; p. 2050313X17745904
Main Authors Umrigar, Ayesha, Musso, Amanda, Mercer, Danielle, Hurley, Annette, Glausier, Cassondra, Bakeer, Mona, Marble, Michael, Hicks, Chindo, Tsien, Fern
Format Report
LanguageEnglish
Published 01.01.2017
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Bibliography:ObjectType-Case Study-2
content type line 59
SourceType-Reports-1
ObjectType-Report-1
ISSN:2050-313X
2050-313X
DOI:10.1177/2050313X17745904