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Low prevalence of MYOC mutations in UK primary open-angle glaucoma patients limits the utility of genetic testing

dc.contributor.authorAldred, MAen_US
dc.contributor.authorBaumber, Len_US
dc.contributor.authorHill, Aen_US
dc.contributor.authorSchwalbe, ECen_US
dc.contributor.authorGob, Ken_US
dc.contributor.authorKarwatowski, Wen_US
dc.contributor.authorTrembath, RCen_US
dc.date.accessioned2016-05-19T13:51:30Z
dc.date.available2004-06-21en_US
dc.date.issued2004-10en_US
dc.identifier.issn0340-6717en_US
dc.identifier.urihttp://qmro.qmul.ac.uk/xmlui/handle/123456789/12438
dc.format.extent428 - 431en_US
dc.relation.ispartofHUM GENETen_US
dc.subjectOPTINEURINen_US
dc.subjectPOPULATIONen_US
dc.subjectTIGRen_US
dc.titleLow prevalence of MYOC mutations in UK primary open-angle glaucoma patients limits the utility of genetic testingen_US
dc.typeArticle
dc.rights.holder© Springer-Verlag 2004.
dc.identifier.doi10.1007/s00439-004-1171-1en_US
pubs.issue5en_US
pubs.notesNot knownen_US
pubs.volume115en_US


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