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Q47138994-34EE85BA-1BAD-4D61-AA8D-C8399F462915
Q47138994-34EE85BA-1BAD-4D61-AA8D-C8399F462915
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47138994-34EE85BA-1BAD-4D61-AA8D-C8399F462915
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.
P2860
Q47138994-34EE85BA-1BAD-4D61-AA8D-C8399F462915
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47138994-34EE85BA-1BAD-4D61-AA8D-C8399F462915
rank
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type
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wasDerivedFrom
6cceb630d1b79de2352ef0a15f0895c00da7b8b3
P2860
GJB2-associated hearing loss: systematic review of worldwide prevalence, genotype, and auditory phenotype.