| pubmed-article:21569298 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:21569298 | lifeskim:mentions | umls-concept:C0271097 | lld:lifeskim |
| pubmed-article:21569298 | lifeskim:mentions | umls-concept:C0017337 | lld:lifeskim |
| pubmed-article:21569298 | lifeskim:mentions | umls-concept:C0332161 | lld:lifeskim |
| pubmed-article:21569298 | lifeskim:mentions | umls-concept:C1513388 | lld:lifeskim |
| pubmed-article:21569298 | lifeskim:mentions | umls-concept:C0015295 | lld:lifeskim |
| pubmed-article:21569298 | lifeskim:mentions | umls-concept:C0205197 | lld:lifeskim |
| pubmed-article:21569298 | lifeskim:mentions | umls-concept:C1561491 | lld:lifeskim |
| pubmed-article:21569298 | lifeskim:mentions | umls-concept:C0205309 | lld:lifeskim |
| pubmed-article:21569298 | pubmed:dateCreated | 2011-6-29 | lld:pubmed |
| pubmed-article:21569298 | pubmed:abstractText | Usher syndrome (USH) combines sensorineural deafness with blindness. It is inherited in an autosomal recessive mode. Early diagnosis is critical for adapted educational and patient management choices, and for genetic counseling. To date, nine causative genes have been identified for the three clinical subtypes (USH1, USH2 and USH3). Current diagnostic strategies make use of a genotyping microarray that is based on the previously reported mutations. The purpose of this study was to design a more accurate molecular diagnosis tool. | lld:pubmed |
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| pubmed-article:21569298 | pubmed:language | eng | lld:pubmed |
| pubmed-article:21569298 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21569298 | pubmed:citationSubset | IM | lld:pubmed |
