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Q47138994-42D2B6D0-EBA1-42BC-89CF-48DB3262A2FD
Q47138994-42D2B6D0-EBA1-42BC-89CF-48DB3262A2FD
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Statement
http://www.wikidata.org/entity/statement/Q47138994-42D2B6D0-EBA1-42BC-89CF-48DB3262A2FD
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
Q47138994-42D2B6D0-EBA1-42BC-89CF-48DB3262A2FD
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47138994-42D2B6D0-EBA1-42BC-89CF-48DB3262A2FD
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wasDerivedFrom
6cceb630d1b79de2352ef0a15f0895c00da7b8b3
P2860
Targeted next-generation sequencing of deafness genes in hearing-impaired individuals uncovers informative mutations.